3-Bromo-4-methylbenzoic acid → HCID 24984145, compound

HRID 2101883Notes

Reaction equation

HRID 2101883 reaction equation
[C:1]([C:3]1[C:4]([C:17]([F:20])([F:19])[F:18])=[C:5]2[C:9](=[CH:10][CH:11]=1)[N:8]([CH2:12][C:13](=[NH:16])[NH:14][OH:15])[CH:7]=[CH:6]2)#[N:2].[Br:21][C:22]1[CH:23]=[C:24]([CH:28]=[CH:29][C:30]=1[CH3:31])[C:25](O)=O>>[Br:21][C:22]1[CH:23]=[C:24]([C:25]2[O:15][N:14]=[C:13]([CH2:12][N:8]3[C:9]4[C:5](=[C:4]([C:17]([F:19])([F:20])[F:18])[C:3]([C:1]#[N:2])=[CH:11][CH:10]=4)[CH:6]=[CH:7]3)[N:16]=2)[CH:28]=[CH:29][C:30]=1[CH3:31]

Participants

3

Reactant 2

HCID 821303-Bromo-4-methylbenzoic acidHCID 178509476HCID 178509476, compound

Product 1

HCID 24984145HCID 24984145, compound

Procedure

Synthesized as described in Example 72 from 2-[5-cyano-4-(trifluoromethyl)-1H-indol-1-yl]-N-hydroxyethanimidamide and 3-bromo-4-methylbenzoic acid: MS (ESI): m/z 461 (M+).

Workup

  1. customSynthesized

Sources & evidence

ORD record
ord-59837864398a4e54841fc6121fd90931
Source dataset
uspto-grants-2009_08
Patent number
US07572820B2

Reaction notes

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