Process for the manufacture of 4-aminobenzoamidine dihydrochloride
The present invention relates to a process for the preparation of 4-aminobenzoamidine (4-AMBA) salts of general formula (I) preferably the salts thereof with hydrochloric or hydrobromic acid, particularly preferred the dichloride salt.
1. A process for the preparation of a compound of formula (I),
wherein n is 1 or 2 and X is Cl or Br, wherein the process comprises reaction step (B):
(B) treating compound (II) with an alcoholic solution of ammonia,
wherein R is methyl, ethyl, propyl, or butyl, and X is Cl or Br.
2. The process for the preparation of a compound of formula (I) according to claim 1 , wherein the process comprising reaction steps (A) and (B):
treating 4-aminobenzonitril (III) with HX in a pure or mixed alcoholic solvent at a reaction pressure of about 0 to 10 atm
to form compound (II)
wherein if R is ethyl, the reaction pressure is between 2 to 6 atm.
3. A process for the preparation of a compound of formula (I),
wherein n is 1 or 2, and X is Cl or Br, wherein the process comprises reaction steps (A), (B), and (C):
treating 4-aminobenzonitril (III) with HX in a pure or mixed alcoholic solvent at a reaction pressure of about 0 to 10 atm
to form compound (II)
wherein if R is ethyl, the reaction pressure is between 2 to 6 atm;
treating compound (II) with an alcoholic solution of ammonia, wherein R is methyl, ethyl, propyl, or butyl, and X is Cl or Br; and (C) precipitating compound (I) by acidification with aqueous HX, wherein the steps (A), (B) and (C) take place successively in the order specified.
4. The process for the preparation of a compound of formula (I) according to one of claims 1 to 3 , wherein the alcoholic solvent or alcoholic solution is ethanolic or methanolic.
5. The process for the preparation of a compound of formula (I) according to one of claims 1 to 3 , wherein the alcoholic solvent or alcoholic solution is methanolic.
6. The process according to claim 3 , wherein the alcoholic solvent or alcoholic solution in steps (A), (B), is the same and is ethanolic or methanolic.
7. The process according to one of claims 1 to 3 , wherein the HCl or HBr in step (A) or step (B) is in a concentration from 5% to 30% (weight %) in alcohol.
8. The process according to one of claims 2 to 3 , wherein a molar ratio of HCl or HBr to compound (III) is from 2:1 to 20:1.
9. The process according to one of claims 2 to 3 wherein the reaction according to step (A) is conducted at a temperature from −10° C. to 80° C.
10. The process according to one of claims 1 to 3 , wherein the step (B) is run at the temperature from 20° C. to 80° C.
11. The process according to one of claims 1 to 3 , wherein the reaction is run in NH 3 in an alcohol solution with a concentration of NH 3 from 5% to 30% (weight %).
12. The process according to one of claims 1 to 3 , wherein the molar ratio of NH 3 to compound (II) is from 2:1 to 20:1.