Ammonia → N-{2-Amino-2-oxo-1-[4-(trifluoromethoxy)benzyl]ethyl}-4-(3,3,3-trifluoropropoxy)benzamide

HRID 1799284

Reaction equation

HRID 1799284 reaction equation
[F:1][C:2]([F:32])([F:31])[O:3][C:4]1[CH:9]=[CH:8][C:7]([CH2:10][CH:11]([NH:15][C:16](=[O:30])[C:17]2[CH:22]=[CH:21][C:20]([O:23][CH2:24][CH2:25][C:26]([F:29])([F:28])[F:27])=[CH:19][CH:18]=2)[C:12](O)=[O:13])=[CH:6][CH:5]=1.[NH3:33]>>[NH2:33][C:12](=[O:13])[CH:11]([NH:15][C:16](=[O:30])[C:17]1[CH:22]=[CH:21][C:20]([O:23][CH2:24][CH2:25][C:26]([F:29])([F:28])[F:27])=[CH:19][CH:18]=1)[CH2:10][C:7]1[CH:8]=[CH:9][C:4]([O:3][C:2]([F:32])([F:31])[F:1])=[CH:5][CH:6]=1

Participants

3

Procedure

A reaction similar to that described in Example 32 (32c) was conducted using 3-[4-(trifluoromethoxy)phenyl]-2-{[4-(3,3,3-trifluoropropoxy)benzoyl]amino}propanoic acid (5.00 g) prepared in Example 70 (70a) and ammonia (16.1 mL, 2 M ethanol solution) to give 4.51 g of the title compound (white powder).

Workup

  1. customA reaction similar to

Sources & evidence

ORD record
ord-c9c6085cd3064732b380c37779ec2ad2
Source dataset
uspto-grants-2013_01
Patent number
US08344029B2

Linked notes

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