3-(Trifluoromethyl)benzeneacetic acid → N-(2-{[1-(2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethyl)-1H-pyrrolo[3,2-c]pyridin-3-yl]carbonyl}pyridin-4-yl)-2-[3-(trifluoromethyl)phenyl]acetamide

HRID 1753035Notes

Reaction equation

HRID 1753035 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([C:8]([C:10]2[C:14]3[CH:15]=[N:16][CH:17]=[CH:18][C:13]=3[N:12]([CH:19]([CH3:29])[CH2:20][O:21][Si:22]([C:25]([CH3:28])([CH3:27])[CH3:26])([CH3:24])[CH3:23])[CH:11]=2)=[O:9])[CH:3]=1.[F:30][C:31]([F:43])([F:42])[C:32]1[CH:33]=[C:34]([CH2:38][C:39](O)=[O:40])[CH:35]=[CH:36][CH:37]=1>>[Si:22]([O:21][CH2:20][CH:19]([N:12]1[C:13]2[CH:18]=[CH:17][N:16]=[CH:15][C:14]=2[C:10]([C:8]([C:4]2[CH:3]=[C:2]([NH:1][C:39](=[O:40])[CH2:38][C:34]3[CH:35]=[CH:36][CH:37]=[C:32]([C:31]([F:42])([F:30])[F:43])[CH:33]=3)[CH:7]=[CH:6][N:5]=2)=[O:9])=[CH:11]1)[CH3:29])([C:25]([CH3:28])([CH3:27])[CH3:26])([CH3:23])[CH3:24]

Participants

3

Procedure

Prepared according to Method Z (Preparation 8) using (4-aminopyridin-2-yl)[1-(2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethyl)-1H-pyrrolo[3,2-c]pyridin-3-yl]methanone (Preparation 30) and 3-trifluoromethylphenylacetic acid.

Workup

  1. customPrepared
  2. customaccording to Method Z (Preparation 8)

Sources & evidence

ORD record
ord-d0f12ddd6f444bd7a2dacb3f9322aaac
Source dataset
uspto-grants-2015_10
Patent number
US09163021B2

Reaction notes

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