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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390619Generated: October 30, 2026

Acetyl chloride → n-[4-(4-Aminothieno[3,2-c]pyridin-3-yl)phenyl]acetamide

https://huagongshe.com/reaction/2390619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant4-MethylmorpholineHCID 7972—
Reactant3-(4-Aminophenyl)thieno(3,2-c)pyridin-4-amineHCID 18450753—
SolventTetrahydrofuranHCID 8028—
Productn-[4-(4-Aminothieno[3,2-c]pyridin-3-yl)phenyl]acetamideHCID 1845135395.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

A −30° C. solution of Example 17A (0.1 g, 0.41 mmol) and N-methylmorpholine (0.03 mL, 0.41 mmol) in THF (5 mL) was treated dropwise with acetyl chloride (0.03 mL, 0.41 mmol), stirred for 1 hour, warmed to 0° C. over 1 hour, quenched with water, and extracted twice with ethyl acetate. The combined extracts were washed with brine, dried (MgSO4), filtered, and concentrated to provide 111 mg of the desired product. Rf=0.24 (5% methanol/dichloromethane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273736B2
Source datasetuspto-grants-2012_09
ORD IDord-ddb5987633a148769b0af9a6fed78df7
Source noteuspto-grants-2012_09