Methods of manufacturing of niraparib
Disclosed herein are methods and processes of preparing niraparib and pharmaceutically acceptable salts thereof, and intermediates and their salts useful for the synthesis of niraparib.
1. A process for preparing a salt of Formula (7),
said process comprising:
(a) a first process that is preparing a compound of Formula (1), or a salt thereof, comprising:
wherein said first process comprises contacting a compound of Formula (2), or a salt thereof, with a compound of Formula (3), or a salt thereof,
wherein:
R 1 is H or an amine protecting group;
R 2 is H, C 1-10 alkyl, C 1 -10 haloalkyl, or aryl; and
each R 3 is independently H, halogen, C 1 -10 alkyl, C 1 -10 haloalkyl, or aryl;
(b) a second process that is a process for preparing a compound of Formula (5), or a salt thereof,
wherein said second process consists of contacting a compound of Formula (1), or a salt thereof, with a copper salt in the presence of THF and toluene solvents,
and
(c) a third process that is a process for preparing a salt of Formula (7),
wherein A is a cation, wherein said third process comprises contacting a compound of Formula (5), or a salt thereof, with a metal hydroxide,
2. The process of claim 1 , wherein the contacting in said first process is in the presence of an acid that is TFA.
3. The process of claim 1 , wherein R 1 is an amine protecting group that is tert-butyloxycarbonyl group (Boc).
4. The process of claim 1 , wherein the compound of Formula (1) has a structure of Formula (4):
5. The process of claim 1 , wherein the copper salt in said second process is copper(II) trifluoromethanesulfonate (Cu(OTf) 2 ).
6. The process of claim 1 , wherein the salt of Formula (7) has a structure of Formula (8):
7. The process of claim 1 , wherein the compound of Formula (5) has a structure of Formula (6):