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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301119Generated: October 25, 2026

Triethylamine → tert-butyl 4H,5H,6H,7H-thieno[3,2-c]pyridine-5-carboxylate

https://huagongshe.com/reaction/2301119

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMono-tert-butyl carbonateHCID 3015642—
Reactant4,5,6,7-Tetrahydrothieno(3,2-c)pyridineHCID 3085076—
SolventDichloromethaneHCID 6344—
Producttert-butyl 4H,5H,6H,7H-thieno[3,2-c]pyridine-5-carboxylateHCID 18377286—

Reaction Steps

4,5,6,7-Tetrahydro-thieno[3,2-c]pyridine (1.3 g, 9.0 mmol) was dissolved in dichloromethane (25 ml), and the solution was mixed with t-butyl bicarbonate (3.1 ml, 13 mmol) and triethylamine (1.3 ml, 9. 0 mmol) and stirred at room temperature for 13 hours. The reaction solution was mixed with dichloromethane, washed with water and saturated brined and dried with anhydrous sodium sulfate. When the solvent was removed by evaporation from the organic layer under a reduced pressure and the thus obtained material was separated and purified by a silica gel column chromatography, it was able to isolate a part of the title compound, but the most part was obtained as its mixture with t-butyl bicarbonate (total yield, 2.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498251B1
Source datasetuspto-grants-2002_12
ORD IDord-6f5f461b37824990be8bbacdf80258d9
Source noteuspto-grants-2002_12