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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247583Generated: October 26, 2026

2,3-Butanediamine → N-(2-amino-1-methylpropyl)-5-isoquinolinesulfonamide

https://huagongshe.com/reaction/247583

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-ButanediamineHCID 136362—
Reactant5-Isoquinolinesulfonyl chlorideHCID 3371655—
SolventChloroformHCID 6212—
ProductN-(2-amino-1-methylpropyl)-5-isoquinolinesulfonamideHCID 2015989280%

Reaction Steps

In 100 ml of chloroform was dissolved 12.9 g of 2,3-diaminobutane and to the solution was added dropwise 10 ml of a chloroform solution containing 4.0 g of 5-isoquinolinesulfonyl chloride under cooling with ice. After the dropwise addition of the chloroform solution, the mixed solution was stirred at a temperature of 20° C. to 25° C. for two hours, and the reaction mixture solution was washed with water and dried with anhydrous sodium carbonate. The chloroform was distilled therefrom under reduced pressure, and the residue thus obtained was subjected to a column chromatography [silica gel: 160 g; solvent: chloroform] to give 3.92 g of N-(2-amino-1-methylpropyl)-5-isoquinolinesulfonamide in a yield of 80%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04709032
Source datasetuspto-grants-1987_11
ORD IDord-af05719e99bc4905b99766affd96dcba
Source noteuspto-grants-1987_11