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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415901Generated: October 29, 2026

Triethylamine → [(Z)-1-aminoethylideneamino] 7-chlorothieno[3,2-b]pyridine-2-carboxylate

https://huagongshe.com/reaction/415901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-HydroxyacetamidineHCID 30926—
Reactant7-Chlorothieno[3,2-b]pyridine-2-carbonyl chlorideHCID 22143543—
SolventChloroformHCID 6212—
Product[(Z)-1-aminoethylideneamino] 7-chlorothieno[3,2-b]pyridine-2-carboxylateHCID 5959839546%

Reaction Steps

A 100 mL round bottom flask was charged with lithium 7-chlorothieno[3,2-b]pyridine-2-carboxylate (0.500 g, 2.28 mmol), methylene chloride (15 ml), and 6 drops of DMF. Oxalyl chloride (0.248 ml, 2.85 mmol) was added dropwise, and the reaction mixture was stirred at room temperature for 3 hours then concentrated in vacuo to yield 7-chlorothieno[3,2-b]pyridine-2-carbonyl chloride as a brown solid. This material was suspended in chloroform (5 mL). N′-hydroxyacetamidine (0.186 g, 2.50 mmol), triethylamine (0.347 ml, 2.50 mmol), and chloroform (15 mL) were stirred together in a 50 mL flask to form a slurry, which was slowly added to the 7-chlorothieno[3,2-b]pyridine-2-carbonyl chloride suspension, then stirred for 1.5 hours at room temperature. The reaction mixture was diluted with chloroform (50 mL) and washed with water (50 mL), sat. aq. NaHCO3 (50 mL) and brine (50 mL). The organic layer was dried with MgSO4, filtered, and concentrated in vacuo. The resulting brown solid was triturated with toluene, and the precipitate collected to obtain the title compound (0.282 g, 46% yield) as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088794B2
Source datasetuspto-grants-2012_01
ORD IDord-ba22fcb24a8544dfb892bc3423638435
Source noteuspto-grants-2012_01