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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494407Generated: November 2, 2026

Isopropanol → (RS)-3-(2-Dimethylaminopropyl)2-imino-6-trifluoromethoxybenzothiazoline

https://huagongshe.com/reaction/1494407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantRiluzoleHCID 5070—
Reactant2-Chloropropyldimethylamine hydrochlorideHCID 94294—
Product(RS)-3-(2-Dimethylaminopropyl)2-imino-6-trifluoromethoxybenzothiazolineHCID 3076394—

Reaction Steps

2-Amino-6-trifluoromethoxybenzothiazole (9.4 g) and 2-chloro-1-dimethylaminopropane hydrochloride (7.0 g) are heated for 1 hour to 130.C. 2-Propanol (20 cc) is added and heating is continued for 24 hours to boiling. After cooling of the mixture to a temperature in the region of 20.C, the precipitate is filtered off and then treated with IN sodium hydroxide (80 cc) in distilled water (100 cc). The residue obtained by extraction with dichloromethane, drying over magnesium sulphate and concentration to dryness under reduced pressure (20 mm Hg; 2.7 kPa) is purified by chromatography on a silica column with a mixture of ethyl acetate and methanol (80:20 by volume) as eluent. (RS)-3-(2-Dimethylaminopropyl)2-imino-6-trifluoromethoxybenzothiazoline (3.3 g) is obtained in the form of a yellow oil, which is converted to a dihydrochloride subliming at about 190° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05026717
Source datasetuspto-grants-1991_06
ORD IDord-a1a7b94c320d4280a5278aaecd1f3e22
Source noteuspto-grants-1991_06