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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483143Generated: November 2, 2026

Methanesulfonyl chloride → HCID 131714589, compound

https://huagongshe.com/reaction/483143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1-(3-Aminophenyl)-1,4-dihydroisoquinol-3-oneHCID 20242553—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 131714589HCID 13171458948.7%

Reaction Steps

A solution of 1-(3-aminophenyl)-1,4-dihydroisoquinol-3-one (8.0 g) in dichloromethane (500 ml) and triethylamine (50 ml) was treated dropwise, at room temperature, with a solution of mesyl chloride (9.7 g) in dichloromethane (20 ml). After stirring for 3 h, the resulting precipitate (m.p. 251°-253° C.) was collected, washed with dichloromethane, water, and air dried. The product was stirred with a mixture of 10% aqueous sodium hydroxide (200 ml) and methanol (20 ml) at 50° C. for 1 h. The mixture was filtered and the filtrate was evaporated to one third volume in vacuo. It was acidified with dilute hydrochloric acid, and the resulting precipitate was collected and washed with water. Recrystallisation from methanol-ether afforded the title compound (3.55 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04578393
Source datasetuspto-grants-1986_03
ORD IDord-4794dafb8d5f4a8babe4dcf675b28e02
Source noteuspto-grants-1986_03