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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36910Generated: October 23, 2026

alpha-chloro-N,N-dimethyl-2-(2,5-dimethylthien-3-yl)imidazo[2,1-b]benzothiazole-3-acetamide hydrochloride → N,N-dimethyl-2-(2,5-dimethylthien-3-yl)imidazo[2,1-b]benzothiazole-3-acetamide

https://huagongshe.com/en/reaction/36910

Reaction equation

Participants

RoleNameHCIDCharge
Reactantalpha-chloro-N,N-dimethyl-2-(2,5-dimethylthien-3-yl)imidazo[2,1-b]benzothiazole-3-acetamide hydrochlorideHCID 19936712—
ReactantSodium Formaldehyde SulfoxylateHCID 23689980—
SolventDichloromethaneHCID 6344—
ProductN,N-dimethyl-2-(2,5-dimethylthien-3-yl)imidazo[2,1-b]benzothiazole-3-acetamideHCID 19936717—

Reaction Steps

34 g (0.077 mole) of α-chloro-N,N-dimethyl-2-(2,5-dimethylthien-3-yl)imidazo[2,1-b]benzothiazole-3-acetamide hydrochloride in solution in 500 ml of dichloromethane are treated with 36.9 g (0.24 mole) of Rongalite®, while stirring the mixture at room temperature for 24 h. The organic phase is separated after settling has taken place, the solid residue is washed with dichloromethane, the organic phase is washed with a saturated sodium hydrogen carbonate solution and then with water, it is dried over sodium sulphate, the solvent is evaporated under reduced pressure and 22 g of solid are obtained. After recrystallization from ethanol and treatment with vegetable black, 17 g of pale yellow crystals are finally obtained. Melting point: 194°-195° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05418248
Source datasetuspto-grants-1995_05
ORD IDord-d92df32fa3c24976935b2b186cc36c14
Source noteuspto-grants-1995_05