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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569049Generated: October 29, 2026

2-Sulfamoyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine → 2-Sulfamoyl-4,5-dihydrothieno[2,3-c]pyridine

https://huagongshe.com/reaction/569049

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Sulfamoyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridineHCID 20148589—
CatalystHCID 178418406HCID 178418406—
SolventEthyl AcetateHCID 8857—
Product2-Sulfamoyl-4,5-dihydrothieno[2,3-c]pyridineHCID 2014858426.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a partial suspension of 2-sulfamoyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine (3.05 g, 14 mmol) in ethyl acetate (200 ml) was added activated manganese dioxide (3.0 g). This mixture was warmed to 80° C. Every two hours an additional 3.0 g of activated manganese dioxide was added until 12 g total had been added. This mixture was filtered hot and the collected manganese dioxide was re-extracted with hot ethyl acetate. The combined ethyl acetate extracts were evaporated to give 2.1 g of crude product. This material was purified by chromatography on silica gel eluting with a gradient 0-5% methanol/ethyl acetate. Recrystallization from ethyl acetate gave pure product (0.8 g, 26.5% yield); m.p. 161°-164° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04731368
Source datasetuspto-grants-1988_03
ORD IDord-6c2faa2194c74971a021659bf646e7f7
Source noteuspto-grants-1988_03