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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432552Generated: October 25, 2026

1,2-Dichloroethane → N-[4-(1-methyl-4,5-dihydro-1H-imidazol-2-yl)phenyl]-5N-(4-chlorophenylaminocarbonyl)-4,5,6,7-tetrahydro-thieno[3,2-c]pyridine-6-carboxamide

https://huagongshe.com/reaction/1432552

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantWaterHCID 962—
Reactant4-(1-Methyl-4,5-dihydro-1H-imidazol-2-yl)-phenylamineHCID 22728876—
Reactant(4-Chlorophenylaminocarbonyl)-4,5,6,7-tetrahydro-thieno[3,2-c]pyridine-6-carboxylic acidHCID 131727718—
SolventDimethylformamideHCID 6228—
ProductN-[4-(1-methyl-4,5-dihydro-1H-imidazol-2-yl)phenyl]-5N-(4-chlorophenylaminocarbonyl)-4,5,6,7-tetrahydro-thieno[3,2-c]pyridine-6-carboxamideHCID 11526092—

Reaction Steps

To a solution of 5N-(4-chlorophenylaminocarbonyl)-4,5,6,7-tetrahydro-thieno[3,2-c]pyridine-6-carboxylic acid (40 mg, 0.12 mmol) and 4-(1-Methyl-4,5-dihydro-1H-imidazol-2-yl)-phenylamine (42 mg, 0.24 mmol) in DMF (3 mL) and H2O (0.5 mL) at room temperature, EDC (68 mg, 0.35 mmol) was added. The mixture was stirred at room temperature overnight. It was concentrated in vacuo. The residue was purified by HPLC to give the titled compound as a powder (25 mg). MS 494.3 and 496.3 (M+H, Cl pattern).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612089B2
Source datasetuspto-grants-2009_11
ORD IDord-cfea6a67daa64563ab23c6c906a058a3
Source noteuspto-grants-2009_11