HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277186Generated: October 31, 2026
HCID 86731245, compound → HCID 86731244, compound
https://huagongshe.com/reaction/2277186
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86731245 | HCID 86731245 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86731244 | HCID 86731244 | 85.3% |
Reaction Steps
A mixture of N-(2,4-bis(benzyloxy)-3-fluorophenyl)-4-(cyclopropylmethoxy)-2,5-difluorobenzamide (2.50 g), 10% palladium-carbon (containing water (50%), 2.00 g) and THF (20 mL) was stirred at room temperature for 30 min under a hydrogen atmosphere. The catalyst was removed by filtration, and the obtained filtrate was concentrated under reduced pressure, and the solid was washed with diethyl ether. To a suspension of the obtained solid, hexachloroethane (2.78 g) and triphenylphosphine (3.08 g) in acetonitrile (20 mL) was added triethylamine (1.96 mL) at 0° C., and the mixture was stirred at room temperature for 15 min, and then with heating at 80° C. for 2 hr. The reaction mixture was filtered, the solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (1.34 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133129B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-752241509d9a4733ad76d8294a582398 |
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| Source note | uspto-grants-2015_09 |
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