HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481849Generated: October 29, 2026
2-Furancarbonyl chloride → HCID 89692820, compound
https://huagongshe.com/reaction/1481849
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Furancarbonyl chloride | HCID 68242 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 89690432 | HCID 89690432 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 89692820 | HCID 89692820 | 50% |
Reaction Steps
To a solution of 5-amino-2-cyclopropyl-N-[3-(2-oxo-pyrrolidin-1-yl)-propyl]-4-(4-o-tolyl-piperazin-1-yl)-benzamide 5b (66.0 mg, 0.14 mmol, 100 mol %) and N,N-diisopropylethylamine (0.07 ml, 0.42 mmol, 300 mol %) in dichloromethane (4.0 ml) was added furan-2-carbonyl chloride (0.02 ml, 0.21 mmol, 150 mol %) and a catalytic amount of N,N-dimethylaminopyridine. The reaction was stirred for 16 h at room temperature and then diluted with water and extracted three times with dichloromethane. The combined organics were dried over sodium sulfate and concentrated to a residue that was purified by column chromatography (dichloromethane to 10% methanol/dichloromethane) to afford furan-2-carboxylic acid [4-cyclopropyl-5-[3-(2-oxo-pyrrolidin-1-yl)-propylcarbamoyl]-2-(4-o-tolyl-piperazin-1-yl)-phenyl]-amide 5d (39.3 mg; 0.07 mmol, 49.7%) as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09409897B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-4c36a59df459488ca84ceab6c38ebfed |
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| Source note | uspto-grants-2016_08 |
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