HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448134Generated: October 29, 2026
Ethyl chloroformate → HCID 178480688, compound
https://huagongshe.com/reaction/448134
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Cumylamine | HCID 68509 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 178480692 | HCID 178480692 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178480688 | HCID 178480688 | 44.9% |
Reaction Steps
To an ice-cooled suspension of 3-([4-(4-methylpiperazin-1-yl)benzoyl]amino}-1H-thieno[2,3-c]pyrazole-5-carboxylic acid (113 mg, 0.27 mmol) and N,N′-diisopropylethylamine (2.1 mmol, 0.38 mL) in 3 mL of N,N-dimethylformamide were added, dropwise, 0.154 mL of ethylchloroformate (1.6 mmol). After 20 minutes, 1-methyl-1-phenyl-ethylamine (0.302 mL, 2.1 mmol) was added to the obtained solution and the reaction mixture was allowed to warm to room temperature. After 16 hours, the reaction mixture was diluted with dichloromethane and washed with an aqueous solution of sodium bicarbonate. After solvent evaporation the residue was taken up with methyl alcohol (9 mL) and triethylamine (1 mL) and stirred at 40° C. for 2 hours. The reaction mixture was then evaporated to dryness to give an oil, which was purified by flash chromatography over silica gel, using dichloromethane/methanol/ammonia 7N solution in methyl alcohol (93:6:1) as eluent, to afford the title compound as a white solid (61 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481584B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-5bfadf0a0d0c4512850d3a92cfbeeec1 |
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| Source note | uspto-grants-2013_07 |
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