Carbamate compounds which inhibit leukocyte adhesion mediated by VLA-4

1. A method for treating a disease selected from the group consisting of asthma, inflammatory bowel disease, ulcerative colitis, Crohn's disease, multiple sclerosis, rheumatoid arthritis, graft versus host disease, and organ or graft rejection in a human or animal subject comprising administering to the human or animal subject a pharmaceutical composition comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound of formula I:

wherein:

Ar is selected from the group consisting of aryl, heteroaryl, substituted aryl, and substituted heteroaryl;

n is an integer from 1 to 4;

X is S or O;

T is selected from the group consisting of a bond, —O—, —S—, —S(O)—, —S(O) 2 —, and —N(R 9 )—, wherein R 9 is selected from the group consisting of hydrogen, alkyl, and substituted alkyl or R 1 and R 9 together with the atoms pendent thereto form a heterocyclic, a substituted heterocyclic, a heteroaryl, or a substituted heteroaryl ring, and provided that when T is —O— or —S— then R 1 is not alkoxy or substituted alkoxy;

R 1 is selected from the group consisting of alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, alkoxy, substituted alkoxy, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclic, and substituted heterocyclic;

R 2 is selected from the group consisting of hydrogen, acyl, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, alkoxy, substituted alkoxy, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclic, and substituted heterocyclic;

or R 1 , R 2 , and T, together with the atoms pendent thereto form a heterocyclic ring consisting of from 4 to 8 ring atoms of the formula:

wherein W is selected from the group consisting of alkylene and substituted alkylene, and wherein one or more of the carbon atoms in the alkylene chain may be replaced by —C(O)—, —C(S)—, —O— or —N(R 10 )— where R 10 is hydrogen, C 1 to C 4 alkyl, or substituted C 1 to C 4 alkyl;

R 3 and R 4 are independently selected from the group consisting of hydrogen, alkyl, substituted alkyl, alkoxy, substituted alkoxy, aryl, substituted aryl, cycloalkyl, substituted cycloalkyl, heteroaryl, substituted heteroaryl, heterocyclic, substituted heterocyclic, and hydroxy; or R 3 and R 4 together with the nitrogen atom to which they are pendent form a heterocyclic or substituted heterocyclic ring;

provided that when one of R 3 and R 4 is hydroxy, alkoxy, or substituted alkoxy the other of R 3 and R 4 is selected from the group consisting of hydrogen, alkyl, substituted alkyl, aryl, substituted aryl, cycloalkyl, substituted cycloalkyl, heteroaryl, substituted heteroaryl, heterocyclic, and substituted heterocyclic;

R 5 is selected from the group consisting of hydrogen, C 1 to C 4 alkyl, and substituted C 1 to C 4 alkyl;

R 6 is selected from the group consisting of carboxy and carboxy ester;

R 7 and R 8 are independently selected from the group consisting of hydrogen, alkyl, and substituted alkyl, or R 7 and R 8 together with the nitrogen atom pendent thereto form a heterocyclic or substituted heterocyclic ring; and

Y is N or CH; or

a pharmaceutically acceptable salt or a pharmaceutically acceptable ester thereof, with the proviso excluding the following compounds as well as their pharmaceutically acceptable salt or ester thereof:

N-[2-diethylamino-5-{N-ethyl-N-(trifluoro acetyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(iso-propylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(t-butylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(furan-2-ylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(piperidin-1-ylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(N-ethyl-N-iso-propylaminocarbonyl)amino}-pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(thien-3-ylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(thien-2-ylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(furan-3-ylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(3-thiapyrrolidin-1-ylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(thien-2-ylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine t-butyl ester;

N-[2-diethylamino-5-{N-ethyl-N-(trifluoromethylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine t-butyl ester;

N-[2-diethylamino-5-{N-ethyl-N-(t-butylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine t-butyl ester; and

N-[2-diethylamino-5-{N-ethyl-N-(furan-3-ylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine t-butyl ester.

2. The method of claim 1 , wherein the compound is of formula II:

wherein:

X is S or O;

T is selected from the group consisting of a bond, —O—, —S—, —S(O)—, —S(O) 2 —, and —N(R 9 )—, wherein R 9 is selected from the group consisting of hydrogen, alkyl, and substituted alkyl or R 1 and R 9 together with the atoms pendent thereto form a heterocyclic, a substituted heterocyclic, a heteroaryl, or a substituted heteroaryl ring, and provided that when T is —O— or —S— then R 1 is not alkoxy or substituted alkoxy;

R 1 is selected from the group consisting of alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, alkoxy, substituted alkoxy, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclic, and substituted heterocyclic;

R 2 is selected from the group consisting of hydrogen, acyl, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, alkoxy, substituted alkoxy, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclic, and substituted heterocyclic;

or R 1 , R 2 , and T, together with the atoms pendent thereto form a heterocyclic ring consisting of from 4 to 8 ring atoms of the formula:

wherein W is selected from the group consisting of alkylene and substituted alkylene, and wherein one or more of the carbon atoms in the alkylene chain may be replaced by —C(O)—, —C(S)—, —O— or —N(R 10 )— where R 10 is hydrogen, C 1 to C 4 alkyl, or substituted C 1 to C 4 alkyl;

R 3 and R 4 are independently selected from the group consisting of hydrogen, alkyl, substituted alkyl, alkoxy, substituted alkoxy, aryl, substituted aryl, cycloalkyl, substituted cycloalkyl, heteroaryl, substituted heteroaryl, heterocyclic, substituted heterocyclic, and hydroxy; or R 3 and R 4 together with the nitrogen atom to which they are pendent form a heterocyclic or substituted heterocyclic ring;

provided that when one of R 3 and R 4 is hydroxy, alkoxy, or substituted alkoxy the other of R 3 and R 4 is selected from the group consisting of hydrogen, alkyl, substituted alkyl, aryl, substituted aryl, cycloalkyl, substituted cycloalkyl, heteroaryl, substituted heteroaryl, heterocyclic, and substituted heterocyclic;

R 5 is selected from the group consisting of hydrogen, C 1 to C 4 alkyl, and substituted C 1 to C 4 alkyl;

R 6 is selected from the group consisting of carboxy and carboxy ester;

R 7 and R 8 are independently selected from the group consisting of hydrogen, alkyl, and substituted alkyl, or R 7 and R 8 together with the nitrogen atom pendent thereto form a heterocyclic or substituted heterocyclic ring; and

Y is N or CH; or

a pharmaceutically acceptable salt or a pharmaceutically acceptable ester thereof.

3. A method for treating a disease selected from the group consisting of asthma, inflammatory bowel disease, ulcerative colitis, Crohn's disease, multiple sclerosis, rheumatoid arthritis, graft versus host disease, and organ or graft rejection in a human or animal subject comprising administering to the human or animal subject a pharmaceutical composition comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound of formula III:

wherein:

X is S or O;

T is selected from the group consisting of a bond, —O—, —S—, —S(O)—, —S(O) 2 —, and —N(R 9 )—, wherein R 9 is selected from the group consisting of hydrogen, alkyl, and substituted alkyl or R 1 and R 9 together with the atoms pendent thereto form a heterocyclic, a substituted heterocyclic, a heteroaryl, or a substituted heteroaryl ring, and provided that when T is —O— or —S— then R 1 is not alkoxy or substituted alkoxy;

R 1 is selected from the group consisting of alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, alkoxy, substituted alkoxy, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclic, and substituted heterocyclic;

R 2 is selected from the group consisting of hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, alkoxy, substituted alkoxy, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, heterocyclic, and substituted heterocyclic;

or R 1 , R 2 , and T, together with the atoms pendent thereto form a heterocyclic ring consisting of from 4 to 8 ring atoms of the formula:

wherein W is selected from the group consisting of alkylene and substituted alkylene, and wherein one or more of the carbon atoms in the alkylene chain may be replaced by —C(O)—, —C(S)—, —O— or —N(R 10 )— where R 10 is hydrogen, C 1 to C 4 alkyl, or substituted C 1 to C 4 alkyl;

R 5 is selected from the group consisting of hydrogen, C 1 to C 4 alkyl, and substituted C 1 to C 4 alkyl;

R 6 is selected from the group consisting of carboxy and carboxy ester;

R 7 and R 8 are independently selected from the group consisting of hydrogen, alkyl, and substituted alkyl, or R 7 and R 8 together with the nitrogen atom pendent thereto form a heterocyclic or substituted heterocyclic ring; and

Y is N or CH; or

a pharmaceutically acceptable salt or a pharmaceutically acceptable ester thereof.

4. The method of claim 3 , wherein the —OC(O)NR 7 R 8 group is in the para position of the phenyl ring.

5. The method of claim 1 , wherein Y is N.

6. The method of claim 1 , wherein X is oxygen.

7. The method of claim 6 , wherein T is a bond and R 1 is selected from the group consisting of methyl, trifluoromethyl, methoxymethyl, ethyl, phenyl, 4-fluorophenyl, 3-fluorophenyl, 2-fluorophenyl, 4-chlorophenyl, 3-chlorophenyl, 2-chlorophenyl, 2,6-dichlorophenyl, benzyl, pyrid-2-yl, pyrid-4-yl, furan-2-yl, furan-3-yl, 3-methylfuran-2-yl, 3-methylthien-2-yl, 5-methyl-thien-2-yl, thien-2-yl, 5-chlorothien-2-yl, 5-(pyrid-2-yl)thien-2-yl, thiazol-2-yl, benzo[b]thien-2-yl, and t-butyl.

8. The method of claim 1 , wherein R 2 is alkyl or substituted alkyl.

9. The method of claim 8 , wherein R 2 is selected from the group consisting of methyl, ethyl, iso-propyl, n-propyl, benzyl, phenethyl, and 4-chlorophenylcarbonylmethyl.

10. The method of claim 1 , wherein R 2 is selected from the group consisting of alkenyl and alkynyl.

11. The method of claim 10 , wherein R 2 is selected from the group consisting of allyl, vinyl, and propargyl.

12. The method of claim 1 , wherein R 3 and R 4 are independently alkyl.

13. The method of claim 12 , wherein R 3 and R 4 are both ethyl.

14. The method of claim 1 , wherein R 5 is hydrogen.

15. The method of claim 1 , wherein n is 1.

16. The method of claim 1 , wherein Ar is selected from the group consisting of phenyl, pyridyl, and pyrimidyl.

17. The method of claim 16 , wherein Ar is phenyl.

18. The method of claim 1 , wherein R 7 and R 8 are each independently alkyl.

19. The method of claim 18 , wherein R 7 /R 8 is selected from the group consisting of methyl/methyl, methyl/ethyl, and ethyl/ethyl.

20. The method of claim 1 , wherein R 7 and R 8 , together with the nitrogen atom to which they are bound, form a heterocyclic ring.

21. The method of claim 20 , wherein the heterocyclic ring is selected from the group consisting of pyrrolidinyl, morpholino, and piperidinyl.

22. A method for treating a disease selected from the group consisting of asthma, inflammatory bowel disease, ulcerative colitis, Crohn's disease, multiple sclerosis, rheumatoid arthritis, graft versus host disease, and organ or graft rejection in a human or animal subject comprising administering to the human or animal subject a pharmaceutical composition comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound selected from the group consisting of:

N-[2-diethylamino-5-{2,5-dioxopyrrolidin-1-yl}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{2-oxopyrrolidin-1-yl}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-methyl-N-methylcarbonylamino}pyrimidin-4-yl]-L-4′-{(dimethylamino)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-isopropyl-N-(methylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(morpholin-4-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-isopropyl-N-(methylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(methylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-methyl-N-(methylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-methylcarbonyl-N-(prop-2-ynyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-methylcarbonyl-N-(prop-2-ynyl)amino}pyrimidin-4-yl]-L-4′-{(dimethylamino)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(methylcarbonyl)amino}pyrimidin-4-yl]-L-4′-}(dimethylamino)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(dimethylaminocarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-methyl-N-(dimethylaminocarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-trifluoromethylcarbonyl-N-isopropylamino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-trifluoromethylcarbonyl-N-isopropylamino}pyrimidin-4-yl]-L-4′-}(dimethylamino)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-isopropyl-N-(dimethylaminocarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(ethylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(methyloxymethylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(pyrrolidin-1-ylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(phenylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(phenyl-methylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(morpholin-4-ylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(2H-5H-pyrrol-1-yl-carbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(diethylaminocarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(N-methyl-N-cyclopentylaminocarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(4-fluorophenylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(3-fluorophenylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(2-fluorophenylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(4-chlorophenylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(3-chlorophenylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(2-chlorophenylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(2,6-dichlorophenylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-trifluoromethyl-carbonyl-N-(prop-2-ynyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(pyridin-2-ylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(pyridin-4-ylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(3-methylfuran-2-ylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-(furan-2-ylcarbonyl)-N-(prop-2-ynyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-prop-2-ynyl-N-(pyrrolidin-1-ylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-trifluoromethyl-carbonyl-N-(2-phenethyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-prop-2-ynyl-N-(thien-2-ylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-(piperidin-1-ylcarbonyl)-N-(prop-2-ynyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-(5-chlorothien-2-ylcarbonyl)-N-ethylamino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-2-phenylethyl-N-(thien-2-ylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-isopropyl-N-(pyrrolidin-1-ylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-phenylmethyl-N-(piperidin-1-ylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-methylcarbonyl-N-(phenylmethyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-phenylmethyl-N-(pyrrolidin-1-ylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(5-methylthien-2-ylcarbonyl)amino}-pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(5-(pyridine-2-yl)thien-2-ylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(thiazol-2-ylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-(4-chlorophenyl-carbonylmethyl)-N-(trifluoromethylcarbonyl)-amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(phenyl-methylaminocarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(1,3-dimethylmorpholin-4-ylcarbonyl)amino}-pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(3,4-dihydroisoquinolin-2(1H)-ylcarbonyl)-amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-(N-cyclohexyl-N-ethylaminocarbonyl)-N-ethylamino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(4-methylpiperidin-1-ylcarbonyl)amino}-pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(N-methyl-N-prop-2-ynylaminocarbonyl)amino}-pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(N-methyl-N-phenylmethylaminocarbonyl)amino}-pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-(benzo[b]thien-2-ylcarbonyl)-N-ethylamino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(phenethylaminocarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-(bicyclo[2.2.1]heptan-2-yl)aminocarbonyl)-N-ethylamino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(3,4-dihydroquinolin-1(2H)-ylcarbonyl)amino}-pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(N-methyl-N-phenylaminocarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(phenylaminocarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(3-methylthien-2-ylcarbonyl)amino}-pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(4-thiomorpholinocarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(N-methyl-N-methoxyaminocarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)-carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(N-methyl-N-phenylaminocarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(N-methyl-N-isoindolin-1-ylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-(N-4-chlorophenyl-N-methylaminocarbonyl)-N-ethylamino}-pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-(N-3-chlorophenyl-N-methylaminocarbonyl)-N-ethylamino}-pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-(cyclohexyl-aminocarbonyl)-N-ethylamino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-(1,3-dioxoisoindolin-2-yl)pyrimidin-4-yl]-L-4′-{(dimethylamino)-carbonyloxy}phenylalanine;

N-[2-diethylamino-5-(1-oxoisoindolin-2-yl)pyrimidin-4-yl]-L-4′-{(dimethylamino)-carbonyloxy}phenylalanine;

N-[2-diethylamino-5-(5,6-dichloro-1,3-dioxoisoindolin-2-yl)pyrimidin-4-yl]-L-4′-{(dimethylamino)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-(N-ethyloxy-carbonylmethyl-N-methylaminocarbonyl)-N-formylamino}pyrimidin-4-yl]-L-4′-{(dimethylamino)carbonyloxy}phenylalanine;

N-[2-diethylamino-5-{N-isopropyl-N-(methylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(dimethylamino)-carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-isopropyl-N-(phenylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(dimethylamino)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-isopropyl-N-(methoxycarbonyl)amino}pyrimidin-4-yl]-L-4′-{(dimethylamino)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-isopropyl-N-(phenyloxycarbonyl)amino}pyrimidin-4-yl]-L-4′-{(dimethylamino)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-phenyl-N-(trifluoromethylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-phenyl-N-(methylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-(3-fluorophenyl)-N-(methylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-(4-fluorophenyl)-N-(methylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-(pyrid-4-yl)-N-(methylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-vinyl-N-(pyrrolidin-1-ylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-(pyrid-3-yl)-N-(methylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(piperidin-1-ylthiocarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

N-[2-diethylamino-5-{N-ethyl-N-(pyrid-4-ylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine t-butyl ester; and

N-[2-diethylamino-5-{N-ethyl-N-(pyrid-4-ylcarbonyl)amino}pyrimidin-4-yl]-L-4′-{(pyrrolidin-1-yl)carbonyloxy}-phenylalanine;

or a pharmaceutically acceptable salt or ester thereof.