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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704225Generated: October 27, 2026

Water → (2RS)-2-(7-chloro-2-cyano-10-phenothiazinyl)propyl methanesulphonate

https://huagongshe.com/reaction/704225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant7-chloro-10-[(2RS)-1-hydroxy-2-propyl]-2-phenothiazinecarbonitrileHCID 15925367—
SolventDichloromethaneHCID 6344—
Product(2RS)-2-(7-chloro-2-cyano-10-phenothiazinyl)propyl methanesulphonateHCID 15925250—

Reaction Conditions

Temperature0 °C

Reaction Steps

Triethylamine (30 cc) is added to a solution of 7-chloro-10-[(2RS)-1-hydroxy-2-propyl]-2-phenothiazinecarbonitrile (40 g) in methylene chloride (400 cc). The mixture is cooled to 0° C. and then treated dropwise in the course of 1 hour with methanesulphonyl chloride (16.6 cc). Distilled water (1 liter) is then added, after which the constituents of the mixture are allowed to settle and the organic phase is separated and washed with distilled water (500 cc). The organic phase is then dried over magnesium sulphate, filtered and concentrated under reduced pressure (30 mm Hg; 4 kPa) to a residual volume of 100 cc. Isopropyl ether (150 cc) is then introduced slowly and the mixture is left stirred for 30 minutes. Isopropyl ether (300 cc) is then added slowly and the suspension is stirred for 48 hours. The precipitate is filtered off, washed with isopropyl ether (2×50 cc) and dried at 40° C. under reduced pressure (5 mm Hg; 0.67 kPa) to give (2RS)-2-(7-chloro-2-cyano-10-phenothiazinyl)propyl methanesulphonate (34.53 g), m.p. 132° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04985419
Source datasetuspto-grants-1991_01
ORD IDord-86e05c2815c14a46aec0bf94ede06c9e
Source noteuspto-grants-1991_01