3,5-Bis(trifluoromethyl)benzoyl chloride → N-(3-Fluoro-[2,4']bipyridinyl-3'-yl)-N-methyl-3,5-bis-trifluoromethyl-benzamide

HRID 878048Notes

Reaction equation

HRID 878048 reaction equation
[F:1][C:2]1[C:3]([C:8]2[CH:13]=[CH:12][N:11]=[CH:10][C:9]=2[NH:14][CH3:15])=[N:4][CH:5]=[CH:6][CH:7]=1.[F:16][C:17]([F:32])([F:31])[C:18]1[CH:19]=[C:20]([CH:24]=[C:25]([C:27]([F:30])([F:29])[F:28])[CH:26]=1)[C:21](Cl)=[O:22]>>[F:1][C:2]1[C:3]([C:8]2[CH:13]=[CH:12][N:11]=[CH:10][C:9]=2[N:14]([CH3:15])[C:21](=[O:22])[C:20]2[CH:19]=[C:18]([C:17]([F:32])([F:31])[F:16])[CH:26]=[C:25]([C:27]([F:30])([F:29])[F:28])[CH:24]=2)=[N:4][CH:5]=[CH:6][CH:7]=1

Participants

3

Procedure

The title compound was prepared in analogy to example 55, from (3-fluoro-[2,4]bipyridinyl-3′-yl)-methyl-amine and 3,5-bis(trifluoromethyl)benzoyl chloride (CAS RN 1271-19-8) and using preparative HPLC for the chromatographic purification. Brown Solid (13%). MS (ESI): m/z=444.4 [M+H]+.

Workup

  1. customfor the chromatographic purification

Sources & evidence

ORD record
ord-a119247750bf4d7ea3052d5c3a8dc563
Source dataset
uspto-grants-2015_03
Patent number
US08987307B2

Reaction notes

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