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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980570Generated: October 27, 2026

4-Piperidino-6-quinazolinesulfonyl chloride → N-(4-aminobutyl)-4-piperidino-6-quinazolinesulfonamide

https://huagongshe.com/reaction/1980570

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Piperidino-6-quinazolinesulfonyl chlorideHCID 13044234—
Reactant1,4-DiaminobuteneHCID 73447540—
SolventChloroformHCID 6212—
ProductN-(4-aminobutyl)-4-piperidino-6-quinazolinesulfonamideHCID 1304423577.5%

Reaction Steps

In 100 ml of chloroform was dissolved 4.4 g of 1,4-diaminobutene, and to the solution was added dropwise 50 ml of a chloroform solution containing 3.1 g of 4-piperidino-6-quinazolinesulfonyl 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 solution was extracted with a 10% aqueous hydrochloric acid solution. The chloroform layer was washed with water and dried with anhydrous potassium carbonate. Then chloroform was distilled from the chloroform layer, and the residue was separated by Prep LC/System 500 (Waters Associates, U.S.A.) [column: Prepack 500/C18 ; solvent: H2O/CH3CN=85/15 (volume ratio); flow rate: 100 ml/minute] to give 2.8 g of N-(4-aminobutyl)-4-piperidino-6-quinazolinesulfonamide [i.e. Compound(31)] as an oily substance in a yield of 77%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04510307
Source datasetuspto-grants-1985_04
ORD IDord-44eadc7e5f8c4e93b68d3b9da50cc8ae
Source noteuspto-grants-1985_04