Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603473Generated: October 30, 2026

Chlorosulfamic acid → 3-(Aminosulfonyl)aminomethylimidazo[5,1-b]thiazole

https://huagongshe.com/reaction/1603473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfamic acidHCID 24499—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Aminomethylimidazo[5,1-b]thiazoleHCID 19605155—
SolventDimethylformamideHCID 6228—
Product3-(Aminosulfonyl)aminomethylimidazo[5,1-b]thiazoleHCID 19605164—

Reaction Conditions

Temperature-25 °C

Reaction Steps

A 770 mg potin of 3-aminomethylimidazo[5,1-b]thiazole was dissolved in 15 ml of DMF, and 4.78 ml of N,N-diisopropylethylamine and 1.04 g of sulfamoyl chloride were further added at -60° C., followed by stirring at -30 to -20° C. for 4 hours. The reaction solution was concentrated under reduced pressure and then dissolved in 30 ml of water, and the solution was adjusted to pH 7.5 with an aqueous sodium hydrogencarbonate solution. After purification by Diaion HP-20 Resin, crystallization was carried out from methanol to obtain 636 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990101
Source datasetuspto-grants-1999_11
ORD IDord-5ccbb9ab523f476e8bb9fe9ba7d8887c
Source noteuspto-grants-1999_11