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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248749Generated: October 29, 2026

Putrescine → N-(4-Aminobutyl)isoquinoline-5-sulfonamide

https://huagongshe.com/reaction/1248749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPutrescineHCID 1045—
Reactant5-Isoquinolinesulfonyl chlorideHCID 3371655—
ReactantChloroform methanolHCID 21584188—
SolventChloroformHCID 6212—
ProductN-(4-Aminobutyl)isoquinoline-5-sulfonamideHCID 1323116262%

Reaction Steps

In 200 ml of chloroform was dissolved 8.8 g of 1,4-diaminobutane, and to the solution was added dropwise 100 ml of a chloroform solution containing 4.55 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 then the reaction solution was extracted with a 10% aqueous hydrochloric acid solution. The pH of the aqueous layer was adjusted to 10 with a 10% aqueous sodium hydroxide solution, and the aqueous layer was extracted with chloroform. The chloroform layer extracted was washed with water and dried with anhydrous potassium carbonate. Then the chloroform was distilled from the chloroform layer, and the residue obtained was subjected to a column chromatography [silica gel: 200 g; developing solvent: 2% methanol/chloroform (volume ratio)] to give 3.46 g of N-(4-aminobutyl)-5-isoquinolinesulfonamide, i.e., Compound (3) as an oily substance in a yield of 62%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04525589
Source datasetuspto-grants-1985_06
ORD IDord-bb6d4ef293ee444aa3b58e2413be48cd
Source noteuspto-grants-1985_06