6-Aminoquinoline → HCID 3281411, compound

HRID 2115369Notes

Reaction equation

HRID 2115369 reaction equation
[N:1]1[C:10]2[C:5](=[CH:6][C:7]([NH2:11])=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[C:12]([C:16]1[CH:21]=[CH:20][C:19]([S:22](Cl)(=[O:24])=[O:23])=[CH:18][CH:17]=1)([CH3:15])([CH3:14])[CH3:13]>>[C:12]([C:16]1[CH:21]=[CH:20][C:19]([S:22]([NH:11][C:7]2[CH:6]=[C:5]3[C:10](=[CH:9][CH:8]=2)[N:1]=[CH:2][CH:3]=[CH:4]3)(=[O:24])=[O:23])=[CH:18][CH:17]=1)([CH3:15])([CH3:13])[CH3:14]

Participants

3

Reactant 2

HCID 113736-AminoquinolineHCID 1398824-t-Butylbenzenesulfonyl chloride

Product 1

HCID 3281411HCID 3281411, compound

Procedure

prepared by reaction of quinolin-6-ylamine with 4-tert-butyl-benzenesulfonyl chloride

Sources & evidence

ORD record
ord-82efdd2e985043b7bbf57bfcfc16278e
Source dataset
uspto-grants-2008_10
Patent number
US07435815B2

Reaction notes

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