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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiophene-3-carboxylic acid | HCID 6918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Methoxy-2-(piperazin-1-yl)pyrimidine | HCID 11480987 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15434276 | HCID 15434276 | 33.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06372746B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-79c7ccc44e42476d8b7a47ac5e839548 |
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| Source note | uspto-grants-2002_04 |
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