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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250745Generated: October 31, 2026

Ethanethiol → 5-Methyl-thiophene-2-carboxylic acid (4-methoxy-7-piperazin-1-yl-benzothiazol-2-yl)-amide

https://huagongshe.com/reaction/2250745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantBoron trifluoride etherateHCID 8000—
Reactant4-{4-Methoxy-2-[(5-methyl-thiophene-2-carbonyl)-amino]-benzothiazol-7-yl}-piperazine-1-carboxylic acid benzyl esterHCID 86584912—
SolventDichloromethaneHCID 6344—
Product5-Methyl-thiophene-2-carboxylic acid (4-methoxy-7-piperazin-1-yl-benzothiazol-2-yl)-amideHCID 8658494258%

Reaction Steps

To a solution of 4-{4-methoxy-2-[(5-methyl-thiophene-2-carbonyl)-amino]-benzothiazol-7-yl}-piperazine-1-carboxylic acid benzyl ester (300 mg, 0.57 mmol) in dichloromethane (5 ml) were added boron trifluoride diethyl etherate (0.72 ml, 5.7 mmol) and ethane thiol (1.2 ml, 17 mmol) and the mixture stirred for 36 h. The volatile components are evaporated and the residue codistilled twice with toluene. The residue was dissolved in dichloromethane (25 ml), extracted with 1N aqueous sodium carbonate and the organic phase dryed with Na2SO4. Removal of the solvent and flash chromatography (silica, eluent CH2Cl2/MeOH/aqu. NH4OH 100:10:1) afforded the title compound as light yellow solid (58%), MS: m/e=389 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07317007B2
Source datasetuspto-grants-2008_01
ORD IDord-67f7a3e316754c788d47a3dcb9878915
Source noteuspto-grants-2008_01