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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197431Generated: November 1, 2026

1-Propanethiol, 2-amino- → 3(R,S)-methyl-7-sulfamoyl-3,4-dihydrothieno[3,2-f]-1,4-thiazepin-5(2H)-one

https://huagongshe.com/reaction/1197431

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Propanethiol, 2-amino-HCID 165845—
ReactantEthyl 2-chloro-5-sulfamoylthiophene-3-carboxylateHCID 19106450—
ReactantPotassium tert-butoxideHCID 23665647—
SolventEthanolHCID 702—
Product3(R,S)-methyl-7-sulfamoyl-3,4-dihydrothieno[3,2-f]-1,4-thiazepin-5(2H)-oneHCID 1910646472.5%

Reaction Steps

To a mixture of potassium tert-butoxide (8.56 g, 0.076 mol) in ethanol (75 mL) was added 2(R,S)-aminopropanethiol (3.1 g, 0.0246 mol) and ethyl 2-chloro-5-sulfamoylthiophene-3-carboxylate (5.98 g, 0.022 mol). The mixture was heated at reflux for 24 hours, and then allowed to stand at room temperature for 24 hours. Following removal of most of the solvent by vacuum concentration, the mixture was acidified to pH 3 with dilute hydrochloric acid. The resulting solids were removed by filtration and dried to give 4.44 g of the title compound, mp 184°-187° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05276025
Source datasetuspto-grants-1994_01
ORD IDord-010f263d5e2e4fe6933dd53dea498f88
Source noteuspto-grants-1994_01