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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720307Generated: November 1, 2026

Dichloromethane → HCID 15290698, compound

https://huagongshe.com/reaction/1720307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant3-Chloropropanesulphonyl chlorideHCID 15410—
ReactantHCID 22923678HCID 22923678—
SolventTriethylamineHCID 8471—
ProductHCID 15290698HCID 15290698—

Reaction Steps

6.6 ml of 3-chloropropanesulfonyl chloride was dropwise added, at 0° C., to a dichloromethane solution containing 8 g of 6-(4-benzylaminobutoxy)carbostyril and 7.6 ml of triethylamine. The mixture was stirred at room temperature for 1 day. The reaction mixture was washed with 10% hydrochloric acid and water in this order and dried with magnesium sulfate. The solvent was removed by distillation. The resulting residue was dissolved in 30 ml of dioxane. To the solution was added 10 ml of a 10% potassium hydroxide solution, followed by stirring at room temperature for 30 minutes. The reaction mixture was neutralized with 10% hydrochloric acid, followed by extraction with chloroform. The extract was dried with magnesium sulfate. The solvent was removed by distillation. The resulting residue was crystallized from diethyl ether to obtain 7.3 g of 6-{4-[N-(3-chloropropylsulfonyl)-N-benzylamino]butoxy}carbostyril.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05506239
Source datasetuspto-grants-1996_04
ORD IDord-b8355eb424b0456bbe76f70a266c3931
Source noteuspto-grants-1996_04