HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102368Generated: October 31, 2026
Cyclopropanecarbonyl chloride → HCID 11539924, compound
https://huagongshe.com/reaction/2102368
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopropanecarbonyl chloride | HCID 77637 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 11646895 | HCID 11646895 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11539924 | HCID 11539924 | 103.6% |
Reaction Steps
A mixture of 3-(3-{[5-(4-fluorophenyl)thieno[2,3-d]pyrimidin-4-yl]oxy}propoxy)aniline (10 mg, 0.025 mmol), diisopropylethylamine (13 mg, 0.10 mmol), and dichloromethane (2 mL) was treated with cyclopropanecarbonyl chloride (30 mg, 0.028 mmol) and stirred at room temperature for 6 hours. The solvent was removed in vacuo and the remaining residue was dissolved in ethyl acetate (25 mL), washed with aqueous sodium bicarbonate solution (2×20 mL), and the organic fraction was separated and concentrated. The product was purified by column chromatography over silica gel using 1% methanol and 0.01% ammonia in 1:1 ethyl acetate/hexanes to give 12 mg (quantitative yield) of N-[3-(3-{[5-(4-fluorophenyl)thieno[2,3-d]pyrimidin-4-yl]oxy}propoxy)phenyl]cyclopropanecarboxamide as a yellow gum. MS [M+H] 464.0,
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07576080B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-b35e5bf44bde4416b10e72ad6f0cbb5f |
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| Source note | uspto-grants-2009_08 |
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