4-Fluoro-2-(trifluoromethyl)benzaldehyde → HCID 86598798, compound

HRID 2104870Notes

Reaction equation

HRID 2104870 reaction equation
[CH2:1]([C:8]1[CH:9]=[N:10][C:11]2[C:16]([C:17]=1[C:18]1[CH:19]=[C:20]([NH2:24])[CH:21]=[CH:22][CH:23]=1)=[CH:15][CH:14]=[CH:13][C:12]=2[C:25]([F:28])([F:27])[F:26])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[F:29][C:30]1[CH:37]=[CH:36][C:33]([CH:34]=O)=[C:32]([C:38]([F:41])([F:40])[F:39])[CH:31]=1>>[CH2:1]([C:8]1[CH:9]=[N:10][C:11]2[C:16]([C:17]=1[C:18]1[CH:19]=[C:20]([NH:24][CH2:34][C:33]3[CH:36]=[CH:37][C:30]([F:29])=[CH:31][C:32]=3[C:38]([F:40])([F:39])[F:41])[CH:21]=[CH:22][CH:23]=1)=[CH:15][CH:14]=[CH:13][C:12]=2[C:25]([F:28])([F:26])[F:27])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

3

Reactant 2

HCID 5229404-Fluoro-2-(trifluoromethyl)benzaldehydeHCID 112342973-(3-Benzyl-8-trifluoromethyl-quinolin-4-yl)-phenylamine

Product 1

HCID 86598798HCID 86598798, compound

Procedure

This compound was prepared according to the procedure of example 66, substituting 3-(3-benzyl-8-trifluoromethyl-quinolin-4-yl)-phenylamine and 4-fluoro-2 trifluoromethyl-benzaldehyde. MS (ESI) m/z 552.

Workup

  1. customThis compound was prepared

Sources & evidence

ORD record
ord-9355f16879db4fec998be42ad5013579
Source dataset
uspto-grants-2009_08
Patent number
US07576215B2

Reaction notes

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