4-Chloro-6,7-diethoxyquinoline-3-carbonitrile → HCID 10206034, compound

HRID 1595817Notes

Reaction equation

HRID 1595817 reaction equation
Cl[C:2]1[C:11]2[C:6](=[CH:7][C:8]([O:15][CH2:16][CH3:17])=[C:9]([O:12][CH2:13][CH3:14])[CH:10]=2)[N:5]=[CH:4][C:3]=1[C:18]#[N:19].[Cl:20][C:21]1[CH:22]=[C:23]([CH:25]=[CH:26][C:27]=1[S:28][C:29]1[N:30]([CH3:34])[CH:31]=[CH:32][N:33]=1)[NH2:24]>>[Cl:20][C:21]1[CH:22]=[C:23]([NH:24][C:2]2[C:11]3[C:6](=[CH:7][C:8]([O:15][CH2:16][CH3:17])=[C:9]([O:12][CH2:13][CH3:14])[CH:10]=3)[N:5]=[CH:4][C:3]=2[C:18]#[N:19])[CH:25]=[CH:26][C:27]=1[S:28][C:29]1[N:30]([CH3:34])[CH:31]=[CH:32][N:33]=1

Participants

3

Reactant 2

HCID 107788724-Chloro-6,7-diethoxyquinoline-3-carbonitrileHCID 114590883-chloro-4-(1-methyl-1H-imidazol-2-ylsulfanyl)phenylamine

Product 1

HCID 10206034HCID 10206034, compound

Procedure

In the manner of Example 141 reaction of 4-chloro-6,7-diethoxy-3-quinolinecarbonitrile with 3-chloro-4-(1-methyl-2-imidazolylthio)aniline (WO-9615118) gave the title compound as a tan solid, mp 285-290° C.

Sources & evidence

ORD record
ord-7ad28c93c2cd4b7cb94e5f54e8b1dfa6
Source dataset
uspto-grants-2001_09
Patent number
US06288082B1

Reaction notes

Loading…