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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111368Generated: October 27, 2026

Riluzole → 2(3H)-Benzothiazolimine, 3-(cyclopropylmethyl)-6-(trifluoromethoxy)-, monohydrobromide

https://huagongshe.com/reaction/1111368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantRiluzoleHCID 5070—
ReactantBromomethylcyclopropaneHCID 81503—
SolventIsopropanolHCID 3776—
Product2(3H)-Benzothiazolimine, 3-(cyclopropylmethyl)-6-(trifluoromethoxy)-, monohydrobromideHCID 30764088.1%

Reaction Conditions

Temperature20 °C

Reaction Steps

The procedure is as in Example 15, starting with 2-amino-6-trifluoromethoxybenzothiazole (9.4 g) and bromomethylcyclopropane (12.7 g) in 2-propanol (30 cc). The mixture is heated for 42 hours to boiling. After cooling of the reaction medium to a temperature in the region of 20° C., the precipitate is filtered off and recrystallized in a boiling mixture (30 cc) of ethyl acetate and methanol (80:20 by volume). 3-Cyclopropylmethyl-2-imino-6-trifluoromethoxybenzothiazoline hydrobromide (1.2 g), m.p. 220° C., is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04980356
Source datasetuspto-grants-1990_12
ORD IDord-e0b04e852d8c41e7a4cdf372b76997f7
Source noteuspto-grants-1990_12