2,4,6-Trifluorobenzaldehyde → {3-[3-Benzyl-8-(Trifluoromethyl)Quinolin-4-yl]Phenyl}(2,4,6-Trifluorobenzyl)Amine

HRID 2104840Notes

Reaction equation

HRID 2104840 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]=[C:36]([F:38])[CH:35]=[C:34]([F:39])[C:31]=1[CH:32]=O>>[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][CH2:32][C:31]3[C:30]([F:29])=[CH:37][C:36]([F:38])=[CH:35][C:34]=3[F:39])[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 5218452,4,6-TrifluorobenzaldehydeHCID 112342973-(3-Benzyl-8-trifluoromethyl-quinolin-4-yl)-phenylamine

Product 1

HCID 86598791{3-[3-Benzyl-8-(Trifluoromethyl)Quinolin-4-yl]Phenyl}(2,4,6-Trifluorobenzyl)Amine

Procedure

This compound was prepared according to the procedure of example 66, substituting 3-(3-benzyl-8-trifluoromethyl-quinolin-4-yl)-phenylamine and 2,4,6 trifluorobenzaldehyde. MS (ESI) m/z 523.

Workup

  1. customThis compound was prepared

Sources & evidence

ORD record
ord-da28a4f0d9aa4d828acc3cc1a66e2c38
Source dataset
uspto-grants-2009_08
Patent number
US07576215B2

Reaction notes

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