2,6-Dichloropyridine-4-carbaldehyde → HCID 86598800, compound

HRID 2104872

Reaction equation

HRID 2104872 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.[Cl:29][C:30]1[CH:35]=[C:34]([CH:36]=O)[CH:33]=[C:32]([Cl:38])[N: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][CH2:36][C:34]3[CH:33]=[C:32]([Cl:38])[N:31]=[C:30]([Cl:29])[CH:35]=3)[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 27610242,6-Dichloropyridine-4-carbaldehydeHCID 112342973-(3-Benzyl-8-trifluoromethyl-quinolin-4-yl)-phenylamine

Product 1

HCID 86598800HCID 86598800, compound

Procedure

This compound was prepared according to the procedure of example 66, substituting 3-(3-benzyl-8-trifluoromethyl-quinolin-4-yl)-phenylamine and 2,6-dichloro-pyridine-4-carbaldehyde. MS (ESI) m/z 535.

Workup

  1. customThis compound was prepared

Sources & evidence

ORD record
ord-a7405565a73a47f3a1346794c818fe03
Source dataset
uspto-grants-2009_08
Patent number
US07576215B2

Linked notes

Loading…