HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874571Generated: October 31, 2026
Cyclopropanecarbonyl chloride → HCID 57385785, compound
https://huagongshe.com/reaction/1874571
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyclopropanecarbonyl chloride | HCID 77637 | — |
| Reactant | HCID 57387818 | HCID 57387818 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 57385785 | HCID 57385785 | 43% |
Reaction Steps
To a solution of N-{3-[(2-aminoimidazo[1,2-a]pyridin-6-yl)oxy]phenyl}-3-(1-cyano-1-methylethyl)benzamide (200 mg, 0.486 mmol) in N,N-dimethylacetamide (2.0 mL) was added cyclopropanecarbonyl chloride (46 μL, 0.510 mmol), and the mixture was stirred at room temperature for 8 hr. The reaction mixture was diluted with ethyl acetate (100 mL), washed with 5% aqueous sodium hydrogen carbonate solution (50 mL) and saturated brine (50 mL), and dried over anhydrous sodium sulfate. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by basic silica gel column chromatography (NH silica gel, hexane/ethyl acetate=50/50→0/100), and fractions containing the desired product were concentrated under reduced pressure. The residue was triturated with ethyl acetate and diisopropyl ether to give the title compound (100 mg, 43%) as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304557B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-2630765f2dd64c8fbc413a08e4e5dd0e |
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| Source note | uspto-grants-2012_11 |
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