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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448132Generated: October 30, 2026

ethyl 5-{[(1-methyl-1-phenylethyl)amino]carbonyl}-3-[(4-morpholin-4-ylbenzoyl)amino]-1H-thieno[2,3-c]pyrazole-1-carboxylate → HCID 178457636, compound

https://huagongshe.com/reaction/448132

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl 5-{[(1-methyl-1-phenylethyl)amino]carbonyl}-3-[(4-morpholin-4-ylbenzoyl)amino]-1H-thieno[2,3-c]pyrazole-1-carboxylateHCID 44520544—
SolventMethanolHCID 887—
SolventTriethylamineHCID 8471—
ProductHCID 178457636HCID 17845763686.7%

Reaction Conditions

Temperature70 °C

Reaction Steps

A suspension of ethyl 5-{[(1-methyl-1-phenylethyl)amino]carbonyl}-3-[(4-morpholin-4-ylbenzoyl)amino]-1H-thieno[2,3-c]pyrazole-1-carboxylate (3.71 g, 6.6 mmol) in methanol (MeOH, 70 mL) and triethylamine (TEA, 7 mL) was stirred at 70° C. for 5 hours. After evaporation of the solvent under reduced pressure, the residue was taken up with DCM and washed with water. The organic layer was separated, dried over sodium sulfate and evaporated. Purification by chromatography (DCM/MeOH 47:3) gave 2.8 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481584B2
Source datasetuspto-grants-2013_07
ORD IDord-08272b04f3f44b5ba8e275b3730bd6e6
Source noteuspto-grants-2013_07