Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494410Generated: October 26, 2026

Riluzole → 3-(2-Acetamidoethyl)-2-imino-6-trifluoromethoxybenzothiazoline

https://huagongshe.com/reaction/1494410

Reaction equation

Participants

RoleNameHCIDCharge
ReactantRiluzoleHCID 5070—
ReactantSodium IodideHCID 5238—
ReactantN-(2-Chloroethyl)acetamideHCID 81815—
SolventMethyl Ethyl KetoneHCID 6569—
Product3-(2-Acetamidoethyl)-2-imino-6-trifluoromethoxybenzothiazolineHCID 307641121.1%

Reaction Conditions

Temperature20 °C

Reaction Steps

2-Amino-6-trifluoromethoxybenzothiazole (9.4 g), N(2-chloroethyl)acetamide (9.7 g) and sodium iodide (13.5 g) in methyl ethyl ketone (30 cc) are heated for 40 hours to boiling. After cooling to a temperature in the region of 20° C., the reaction medium is added to distilled water (200 cc), treated with IN sodium hydroxide (40 cc) and then extracted with ethyl acetate (200 cc). After drying over magnesium sulphate and then concentration to dryness at 40° C. under reduced pressure (20 mm Hg; 2.7 kPa), the residue is purified by chromatography on a silica column with a mixture of ethyl acetate and methanol (90:10 by volume) as eluent. 3-(2-Acetamidoethyl)-2-imino-6-trifluoromethoxybenzothiazoline (2.7 g) is obtained, which product is converted to a hydrochloride subliming at about 180° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05026717
Source datasetuspto-grants-1991_06
ORD IDord-834f28866e1046d99f9122dd971a08ff
Source noteuspto-grants-1991_06