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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1868328Generated: October 26, 2026

Dichloromethane → 1-(4-Amino-2-phenyl-thieno[3,2-c]pyridin-7-yl)-ethanone

https://huagongshe.com/reaction/1868328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
Reactant4-MethoxybenzylamineHCID 75452—
Reactant1-(4-Chloro-2-phenyl-thieno[3,2-c]pyridin-7-yl)-ethanoneHCID 18446512—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
Product1-(4-Amino-2-phenyl-thieno[3,2-c]pyridin-7-yl)-ethanoneHCID 10265028—

Reaction Conditions

Temperature55 °C

Reaction Steps

To a suspension of 1-(4-chloro-2-phenyl-thieno[3,2-c]pyridin-7-yl)-ethanone 97 (61 mg, 0.21 mmol) and potassium carbonate (174 mg, 1.26 mmol) in DMF (1.8 mL) was added 4-methoxybenzylamine (85 μl, 0.64 mmol). The resultant mixture was heated at 50° C. for 6.75 h. After this time, 20 mL of a 1:1 mixture of dichloromethane and methanol was added and the resultant slurry was filtered. The filtrate was concentrated and the residue was dissolved in trifluoroacetic acid (7 mL). The resultant mixture was heated at 55° C. for 2.75 h. After this time, the reaction mixture was concentrated and the residue was purified by silica gel column chromatography (eluent: dichloromethane:MeOH:Et3N, 98.5:1.5:0.5) to give 98.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07635695B2
Source datasetuspto-grants-2009_12
ORD IDord-d145112c00254d549092af405f18581f
Source noteuspto-grants-2009_12