2-Chloro-5-nitroquinoline → HCID 91147090, compound

HRID 1170129Notes

Reaction equation

HRID 1170129 reaction equation
[N+:1]([C:4]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:5]=1[CH:6]=[CH:7][C:8](Cl)=[N:9]2)([O-])=O.[Cl:15][C:16]1[S:20][C:19]([S:21](Cl)(=[O:23])=[O:22])=[CH:18][CH:17]=1.[CH3:25][O:26][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=1[CH:33]([NH2:35])[CH3:34]>>[CH3:25][O:26][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=1[CH:33]([NH:35][C:8]1[CH:7]=[CH:6][C:5]2[C:10](=[CH:11][CH:12]=[CH:13][C:4]=2[NH:1][S:21]([C:19]2[S:20][C:16]([Cl:15])=[CH:17][CH:18]=2)(=[O:23])=[O:22])[N:9]=1)[CH3:34]

Participants

4

Reactant 3

HCID 3192512-Chloro-5-nitroquinolineHCID 27339255-Chlorothiophene-2-sulfonyl chlorideHCID 27942301-(2-Methoxy-phenyl)-ethylamine

Product 1

HCID 91147090HCID 91147090, compound

Procedure

The title compound, MS: m/e=474.1 (M+H+), was prepared in accordance with the general method of example 61 from 5-nitro-2-chloroquinoline, 5-chlorothiophene-2-sulfonylchloride and rac-1-(2-methoxy-phenyl)-ethylamine.

Sources & evidence

ORD record
ord-5dae45efa94e423bb60b8b3fd3525ec1
Source dataset
uspto-grants-2010_11
Patent number
US07825253B2

Reaction notes

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