5-Aminoisoquinoline → HCID 3417981, compound

HRID 2115371Notes

Reaction equation

HRID 2115371 reaction equation
[CH:1]1[C:10]2[C:5](=[C:6]([NH2:11])[CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][N: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:6]2[CH:7]=[CH:8][CH:9]=[C:10]3[C:5]=2[CH:4]=[CH:3][N:2]=[CH:1]3)(=[O:24])=[O:23])=[CH:18][CH:17]=1)([CH3:15])([CH3:13])[CH3:14]

Participants

3

Reactant 2

HCID 707665-AminoisoquinolineHCID 1398824-t-Butylbenzenesulfonyl chloride

Product 1

HCID 3417981HCID 3417981, compound

Procedure

prepared by reaction of isoquinolin-5-ylamine with 4-tert-butyl-benzenesulfonyl chloride

Sources & evidence

ORD record
ord-b43b57d3850149bf9ad2c9582a1372f2
Source dataset
uspto-grants-2008_10
Patent number
US07435815B2

Reaction notes

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