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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494411Generated: October 30, 2026

Iodoacetamide → 2-[2-Imino-6-(trifluoromethoxy)-1,3-benzothiazol-3(2H)-yl]ethanimidic acid

https://huagongshe.com/reaction/1494411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoacetamideHCID 3727—
ReactantRiluzoleHCID 5070—
SolventMethyl Ethyl KetoneHCID 6569—
Product2-[2-Imino-6-(trifluoromethoxy)-1,3-benzothiazol-3(2H)-yl]ethanimidic acidHCID 307641253%

Reaction Steps

The procedure is as in Example 15, starting with 2-amino-6-trifluoromethoxybenzothiazole (9.4 g) and iodoacetamide (14.8 g) in methyl ethyl ketone (50 cc). The mixture is heated for 18 hours to boiling and then cooled to a temperature in the region of 20.C. The precipitate formed is filtered off, then added to distilled water (100 cc) and treated with IN sodium hydroxide (37 cc). The insoluble matter is filtered off, washed with distilled water (100 cc) and recrystallized in boiling methanol (100 cc). (2-Imino-6-trifluoromethoxy-3-benzothiazolinyl)acetamide (6.2 g), m.p. 228° C., is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05026717
Source datasetuspto-grants-1991_06
ORD IDord-57ce784e5da44225a5279cacdcf53993
Source noteuspto-grants-1991_06