Stabilized activated derivatives of carbamic acid, their process of preparation and their use for the preparation of ureas
View Patent ↗Process for the preparation of stable activated derivatives of carbamic acid, comprising at least one protected amino group and an activated carbamic acid function, from an amino acid derivative in which the amino group is protected. The process includes: a) a step of transformation of the —COOH group of the amino acid derivative into a —CON 3 group to obtain an acyl azide; b) a step of transformation of the —CON 3 group of the acyl azide into a —NCO group to obtain an isocyanate; c) a step of treating the isocyanate to obtain a stable derivative of carbamic acid.
1. A compound having the formula (I bis)
wherein
“n” is 1 or 2,
“i” is a whole number varying from 2 to n+1,
GP is selected from the group consisting of:
an oxycarbonyl group ROCO, R representing an alkyl group of 1 to 20 carbon atoms, unsubstituted or substituted with an aryl group whose cyclic structure contains 5 to 20 carbon atoms, said alkyl group being saturated or not,
an acyl group RCO, R being chosen from: an alkyl group of 1 to 20 carbon atoms or an aryl group whose cyclic structure contains 5 to 20 carbon atoms, said alkyl group being possibly substituted with an aryl group whose cyclic structure contains 5 to 20 carbon atoms, said alkyl group being saturated or not,
GP along with R 1 and the N then are bonded to form a phthalimido group of formula:
a biotinyle group having the following formula
groups R 1 and R i can each represent independently from each other: a hydrogen, a halogen, the protected or unprotected side chain of an amino acid selected from natural and synthetic amino acids, a (C 1 –C 20 ) alkyl group, unsubstituted or substituted, an aryl group whose cyclic structure contains 5 to 20 carbon atoms, a group OR a , —NH 2 , —OH, —COOR a , —CONHR a , —CONH 2 , —CH 2 COOR a , —CH 2 CONHR a , —CH 2 CONH 2 ,
R a representing an alkyl group, saturated or not, having 1 to 20 carbon atoms, an aralkyl group having 1 to 20 carbon atoms, or an aryl group whose cyclic structure contains 5 to 20 carbon atoms,
R 1 and R i groups can also form a cycle with N, said cycle being selected from the group consisting of
X group represents a group having one of the following formula:
wherein said compound is not one of the following compounds selected from the group consisting of:
n=2, GP=Boc, R 1 =isobutyl, R 2 =R 3 =H, X=4-nitrophenol;
n=2, GP=Boc, R 1 =benzyl, R 2 =R 3 =H, X=4-nitrophenol;
n=2, GP=Boc, R 1 =CH 2 -p-C 6 H 4 Ot-Bu, R 2 =R 3 =H, X=4-nitrophenol;
n=2, GP=Boc, R 1 =H, R 2 =R 3 =H, X=4-nitrophenol.
2. The compound according to claim 1 , wherein GP represents an oxycarbonyl group chosen from Boc, Fmoc, benzyloxycarbonyl or allyloxycarbonyl.
3. The compound according to claim 1 , in which X is a N-hydroxysuccinimide group and has the following formula:
4. The compound according to claim 1 , wherein the alkyl group corresponding to R 1 or R i is substituted with one or several substituents selected from the group consisting of —COOR h , —CONHR h , —COOH, —OH, —OR h , —NHR h , —NH 2 , —NH(CO)R h , an aryl group whose cyclic structure contains 5 to 20 carbon atoms, halogen, carbonyl, nitrile, and guanidino,
R h representing an alkyl group, saturated or not, having 1 to 20 carbon atoms, an aralkyl group having 1 to 20 carbon atoms, or an aryl group whose cyclic structure contains 5 to 20 carbon atoms.
5. The compound according to claim 1 , having the following formula
wherein R 2 represents a (C 1 –C 20 ) alkyl group, optionally substituted with a phenyl group, and wherein said phenyl group is optionally substituted with an alkoxy group.
6. The compound according to claim 1 , having the following formula:
wherein R 2 represents a (C 1 –C 20 ) alkyl group, optionally substituted with a pvhenyl group, and wherein said phenyl group is optionally substituted with an alkoxy group.
7. A compound having the following formula:
8. A process for preparing a compound according to claim 1 , comprising:
providing a compound of formula (IX)
transforming said compound (IX) into a corresponding acyl azide (XII)
transforming said acyl azide (XII) by Curtius rearrangement into a corresponding isocyanate (II),
treating said isocyanate (II) under conditions that provide a carbamic acid compound of formula (I bis).
9. The process according to claim 8 , wherein transforming said compound (IX) into a corresponding acyl azide (XII) is carried out by treatment of a mixed anhydride, formed by the reaction of acid compound (IX) with ethyl or isobutyl chloroformiate in the presence of a tertiary amine, wherein said tertiary amine is NMM (N-methylmorpholine), DIEA (di-isopropylethylamine), or Et 3 N in THF (tetrahydrofurane) with a sodium azide solution,
wherein said step of transforming acyl azide (XII) into a corresponding isocyanate (II), is carried out by heating a solution of acyl azide in a solvent, and
wherein a compound selected from the group consisting of N-hydroxysuccinimide is the compound treating isocyanate (II) to obtain a carbamic acid derivative of formula (I bis).
10. A compound having the formula (I bis)
wherein
“n” is 1 or 2,
“i” is a whole number varying from 2 to n+1,
GP is selected from the group consisting of:
an oxycarbonyl group ROCO, R representing an alkyl group of 1 to 20 carbon atoms, unsubstituted or substituted with an aryl group whose cyclic structure contains 5 to 20 carbon atoms, said alkyl group being saturated or not,
an acyl group RCO, R being chosen from: an alkyl group of 1 to 20 carbon atoms or an aryl group whose cyclic structure contains 5 to 20 carbon atoms, said alkyl group being possibly substituted with an aryl group whose cyclic structure contains 5 to 20 carbon atoms, said alkyl group being saturated or not,
GP along with R 1 and the N then are bonded to form a phthalimido group of formula:
a biotinyle group having the following formula
groups R 1 and R i can each represent independently from each other: a hydrogen, a halogen, the protected or unprotected side chain of an amino acid selected from natural and synthetic amino acids, a (C 1 –C 20 ) alkyl group, unsubstituted or substituted, an aryl group whose cyclic structure contains 5 to 20 carbon atoms, a group OR a , —NH 2 , —OH, —COOR a , —CONHR a , —CONH 2 , —CH 2 COOR a , —CH 2 CONHR a , —CH 2 CONH 2 ,
R a representing an alkyl group, saturated or not, having 1 to 20 carbon atoms, an aralkyl group having 1 to 20 carbon atoms, or an aryl group whose cyclic structure contains 5 to 20 carbon atoms,
wherein R 1 R i groups can also form a cycle with N, said cycle being selected from the group consisting of
X group represents O-succinimidyl, wherein said compound is not one of the following compounds selected from the group consisting of:
n=2, GP=Boc, R 1 =isobutyl, R 2 =R 3 =H, X=4-nitrophenol;
n=2, GP=Boc, R 1 =benzyl, R 2 =R 3 =H, X=4-nitrophenol;
n=2, GP=Boc, R 1 =CH 2 -p-C 6 H 4 Ot-Bu, R 2 =R 3 =H, X=4-nitrophenol;
n=2, GP=Boc, R 1 =H, R 2 =R 3 =H, X=4-nitrophenol.
11. The compound according to claim 10 , wherein GP represents an oxycarbonyl group chosen from Boc, Fmoc, benzyloxycarbonyl or allyloxycarbonyl.
12. The compound according to claim 10 , wherein X is a O-succinimidyl.
13. The compound according to claim 10 , wherein the alkyl group corresponding to R 1 or R i is substituted with one or several substituents selected from the group consisting of —COOR h , —CONHR h , —COOH, —OH, —OR h , —NHR h , —NH 2 , —NH(CO)R h , an aryl group whose cyclic structure contains 5 to 20 carbon atoms, halogen, carbonyl, nitrile, and guanidino,
R h representing an alkyl group, saturated or not, having 1 to 20 carbon atoms, an aralkyl group having 1 to 20 carbon atoms, or an aryl group whose cyclic structure contains 5 to 20 carbon atoms.