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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69558Generated: October 26, 2026

Water → Imidazo (2,1-b)-1,3,4-thiadiazole, 2-(methoxymethyl)-6-(trifluoromethyl)-

https://huagongshe.com/reaction/69558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-Bromo-1,1,1-trifluoro-2-propanoneHCID 79008—
Reactant5-(Methoxymethyl)-1,3,4-thiadiazol-2-amineHCID 660844—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductImidazo (2,1-b)-1,3,4-thiadiazole, 2-(methoxymethyl)-6-(trifluoromethyl)-HCID 6711708547%

Reaction Conditions

Temperature80 °C

Reaction Steps

Bromotrifluoroacetone (478 g, 1.05 eq) is added on a suspension of 5-(methoxymethyl)-1,3,4-thiadiazol-2-amine a25 (346 g, 1 eq) in 1,2-dimethoxyethane (6 l) at 20° C. The reaction mixture is heated to 80° C. until maximum conversion (<24 h). Water (4 l) is added to the reaction mixture at 32° C. and the expected compound crystallized out of the reaction mixture. The crystalline suspension is cooled to 10° C. to complete the crystallization process, filtered and the crystalline precipitate is washed with water (1.5 l) to afford 266 g of pure 2-(methoxymethyl)-6-(trifluoromethyl)imidazo[2,1-b][1,3,4]thiadiazole a28.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822508B2
Source datasetuspto-grants-2014_09
ORD IDord-517397c5837b4522bbf3990d126ad048
Source noteuspto-grants-2014_09