3-(8-Chloro-3-phenyl-cinnolin-4-yl)-phenylamine → [3-(8-Chloro-3-phenylcinnolin-4-yl)phenyl][5-chloro-2-(trifluoromethyl)benzyl]amine

HRID 643317

Reaction equation

HRID 643317 reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[N:9][C:8]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)=[C:7]2[C:18]1[CH:19]=[C:20]([NH2:24])[CH:21]=[CH:22][CH:23]=1.[Cl:25][C:26]1[CH:27]=[CH:28][C:29]([C:34]([F:37])([F:36])[F:35])=[C:30]([CH:33]=1)[CH:31]=O>>[Cl:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[N:9][C:8]([C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1)=[C:7]2[C:18]1[CH:19]=[C:20]([NH:24][CH2:31][C:30]2[CH:33]=[C:26]([Cl:25])[CH:27]=[CH:28][C:29]=2[C:34]([F:36])([F:35])[F:37])[CH:21]=[CH:22][CH:23]=1

Participants

3

Procedure

The title compound was prepared from 3-(8-chloro-3-phenyl-cinnolin-4-yl)-phenylamine and 5-chloro-2-trifluoromethylbenzaldehyde according to the procedure of Step 5 Example 6. MS (ES) m/z 523.9.

Sources & evidence

ORD record
ord-3610b227ac13408fb28a1f23f1d5b06d
Source dataset
uspto-grants-2010_04
Patent number
US07700595B2

Linked notes

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