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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841914Generated: November 1, 2026

Thiophene-3-carboxylic acid → HCID 15434276, compound

https://huagongshe.com/reaction/841914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophene-3-carboxylic acidHCID 6918—
ReactantTriethylamineHCID 8471—
Reactant4-Methoxy-2-(piperazin-1-yl)pyrimidineHCID 11480987—
SolventDichloromethaneHCID 6344—
ProductHCID 15434276HCID 1543427633.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1.0 g (7.81 mmol) of 3-thienylcarboxylic acid and 1 mL (7.86 mmol) of triethylamine in 30 mL of CH2Cl2 cooled to 0° C. 0.84 g (7.81 mmol) of ethyl chloroformiate are added. The mixture is maintained at 0° C. for 20 minutes and then 1.5 g (7.81 mmol) of 4-methoxy-2-(1-piperazinyl) pyrimidine dissolved in 10 mL of CH2Cl2 are added to the solution. The temperature is allowed to rise to room temperature and the solution continually stirred for 2 hours and the organic phase is washed with H2O, dried over NaSO4 and the solvent evaporated off under reduced pressure. The resulting oil is treated with ethyl ether to yield a solid which is recrystallised from ethanol/H2O to give 0.8 g (2.63 mmol) of 4-methoxy-2-[4-(3-thienylcarbonyl)-1-piperazinyl]pyrimidine. m.p.=90-92° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06372746B1
Source datasetuspto-grants-2002_04
ORD IDord-79c7ccc44e42476d8b7a47ac5e839548
Source noteuspto-grants-2002_04