Processes for preparing 1,2-substituted cyclopropyl derivatives
View Patent ↗The present invention relates to processes for preparing enantiomerically pure cyclopropyl amine derivatives and salts thereof; the chiral intermediates such as the chiral salts are useful for the preparation of such chiral compounds and salts; pharmaceutical compositions comprising the compounds and salts; and method of using such compositions. The chiral cyclopropyl amine derivatives are useful for binding to histamine H 3 receptor sites and for providing therapeutic agents for histamine H 3 mediated disease.
1. A process for preparing a chiral compound of formula:
wherein R 2 , R 3 , R 3a , and R 3b , are hydrogen; R 1 is a 5- to 6-membered heteroaryl ring, cyanophenyl, a 8- to 12-membered bicyclic heteroaryl ring, or a 4- to 12-membered heterocyclic ring; and R 4 and R 5 taken together with the nitrogen atom to which they are attached form an amine moiety represented by structure:
wherein R 7 , R 8 , R 9 , and R 10 at each occurrence are independently selected from the group consisting of hydrogen, hydroxyalkyl, fluoroalkyl, cycloalkyl, and alkyl; R x and R y are each independently selected from the group consisting of hydrogen, hydroxy, alkyl, alkoxy, alkylamino, fluoro, and dialkylamino; and m is an integer from 1 to 5;
comprising the steps of:
a) providing enantiomerically pure chiral salts using chiral resolution with a chiral amine:
wherein the chiral amine is selected from the group consisting of R-(−)-1-cyclohexylethylamine, (R)-(+)-α-methylbenzylamine, (S)-(−)-α-methylbenzylamine, (R)-(+)-N-benzyl-α-methylbenzylamine, (S)-(−)-N-benzyl-α-methylbenzylamine, (R)-(+)-N,N-dimethyl-1-phenylethylamine, (S)-(−)-N,N-dimethyl-1-phenylethylamine, [R-(R*,R*)]-(+)-bis(α-methylbenzyl)amine, [S-(R*,R*)]-(−)-bis(α-methylbenzyl)amine, (S)-(+)-1-cyclohexylethylamine, (R)-(+)-1-(1-naphthyl)ethylamine, (S)-(−)-1-(1-naphthyl)ethylamine, (1R,2R,3R,5S)-(−)-isopinocamphenylamine, (1S,2S,3S,5R)-(+)-isopinocamphenylamine, (1R2R)-(−)-pseudoephedrine, (1S,2S)-(+)-pseudoephedrine, (1R,2S)-(−)-ephedrine, (1S,2R)-(+)-ephedrine, (1R,2S)-(−)-N-methylephedrine, (1S,2R)-(+)-N-methylephedrine, (1R,2S)-(−)-norephedrine, (1S,2R)-(+)-norephedrine, (1R,2S)-(+)-cis-1-amino-2-indanol, (1S,2R)-(−)-cis-1-amino-2-indanol, quinine, and cinchonine;
b) reacting the chiral pure arylcyclopropanecarboxylic acid after released from the chiral salt obtained from chiral resolution with an amine of formula:
wherein R 7 , R 8 , R 9 , and R 10 at each occurrence are independently selected from the group consisting of hydrogen, hydroxyalkyl, fluoroalkyl, cycloalkyl, and alkyl; R x and R y are each independently selected from the group consisting of hydrogen, hydroxy, alkyl, alkoxy, alkylamino, fluoro, and dialkylamino; and m is an integer from 1 to 5; and N,N′-carbonyldiimidazole in tetrahydrofuran to provide a chiral compound of structure:
wherein X is chloro, bromo, iodo, or trifluoromethanesulfonate, and the amine moiety in the structure above is represented by:
wherein R 7 , R 8 , R 9 , and R 10 at each occurrence are independently selected from the group consisting of hydrogen, hydroxyalkyl, fluoroalkyl, cycloalkyl, and alkyl; R x and R y are each independently selected from the group consisting of hydrogen, hydroxy, alkyl, alkoxy, alkylamino, fluoro, and dialkylamino; and m is an integer from 1 to 5;
c) reducing the product of step b to provide a compound of structure:
wherein X and the amine moiety are as described above for compounds of step b); and d) treating the product of step c with a reagent selected from the group consisting of 5- to 6-membered heteroaryl, 8- to 12-membered bicyclic heteroaryl, 4- to 12-membered heterocycloalkyl, N,N′-dimethylethylenediamine, a copper catalyst, and base, in a basic solvent; to provide a compound of formula (II).
2. The process of claim 1 , the chiral amine is R-(−)-1-cyclohexylethylamine and (R)-(+)-α-methylbenzylamine.
3. The process of claim 1 , wherein the amine of formula (a) in step b) is pyrrolidine, 2-R-methylpyrrolidine, 2-S-methylpyrrolidine, or 3-methylpyrrolidine.
4. The process of claim 1 , wherein the compound of structure (1-a) is reduced using borane.
5. The process of claim 4 , wherein the borane reagent is borane or diborane.
6. The process of claim 1 , wherein the compound of structure (I-a) is reduced using borane in a polar solvent.
7. The process of claim 6 , wherein the polar solvent is tetrahydrofuran.
8. The process of claim 6 , wherein the non-polar solvent is toluene.
9. The process of claim 1 , wherein the copper catalyst in step d) is copper (I) iodide.
10. The process of claim 1 , wherein the copper catalyst in step d) is copper (I) bromide or copper (I) chloride.
11. The process of claim 1 , wherein the base in step d) is potassium carbonate (K 2 CO 3 ).
12. The process of claim 1 , wherein the base in step d) is potassium phosphate (K 3 PO 4 ).
13. The process of claim 1 , wherein the base is step d) is cesium carbonate (Cs 2 CO 3 ), sodium methoxide (NaOMe), sodium tert-butoxide (NaOt-Bu), sodium acetate (NaOAc), potassium tert-butoxide (KOt-Bu).
14. The process of claim 1 , wherein the polar aprotic solvent in step d) is pyridine.
15. The process of claim 1 , wherein the polar aprotic solvent in step d) is dimethyl acetamide, dimethyl formamide, or 1-methyl-2-pyrrolidinone.
16. A compound of formula:
wherein the amine moiety in the structure above is represented by:
wherein R 7 , R 8 , R 9 , and R 10 at each occurrence are independently selected from the group consisting of hydrogen, hydroxyalkyl, fluoroalkyl, cycloalkyl, and alkyl; R x and R y are each independently selected from the group consisting of hydrogen, hydroxy, alkyl, alkoxy, alkylamino, fluoro, and dialkylamino; and m is an integer from 1 to 5.