HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16688Generated: October 29, 2026
Acetyl chloride → HCID 178474794, compound
https://huagongshe.com/reaction/16688
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178483799 | HCID 178483799 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 178474794 | HCID 178474794 | — |
Reaction Steps
3-[({Trans-4-[(3-aminopropyl)(methyl)amino]cyclohexyl}-carbonyl)amino]-N-(5-chloropyridin-2-yl)furo[3,2-b]pyridine-2-carboxamide (113 mg) obtained in Example 121 and triethylamine (65 μl) are dissolved in chloroform (5 ml), and thereto is added acetyl chloride (25 μl) under ice-cooling. The mixture is warmed to room temperature and stirred for 1 hour. To the reaction solution is poured saturated aqueous sodium hydrogen carbonate solution, and the mixture is extracted with chloroform. The organic layer is washed successively with water and saturated brine, dried over sodium sulfate, and the solvent is evaporated under reduced pressure. The resulting residue is purified by NH-silica gel column chromatography (eluent: ethyl acetate followed by ethyl acetate/methanol=10/1). The resulting solid is suspended in n-hexane-diisopropyl ether, and collected by filtration to give the title compound (90 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07737161B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-231f1469e8774c6289990276e490ee84 |
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| Source note | uspto-grants-2010_06 |
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