HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56811Generated: October 30, 2026
tert-Butyl 2-[4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-3-(2,2-difluorocyclopropyl)prop-2-enoate → HCID 117622748, compound
https://huagongshe.com/reaction/56811
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-Butyl 2-[4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-3-(2,2-difluorocyclopropyl)prop-2-enoate | HCID 118877865 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | HCID 117622748 | HCID 117622748 | — |
Reaction Steps
At RT, 240 mg (purity 78%, 404 μmol) of tert-butyl 2-[4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-3-(2,2-difluorocyclopropyl)prop-2-enoate (diastereomer mixture) were admixed with 30 ml of a “Hot Stryker's” reagent solution [B. A. Baker et al. Org. Lett. 2008, 10, 289-292]. The reaction mixture was stirred at RT for 2 h, and 20 ml of saturated aqueous ammonium chloride solution were then added. The phases were separated and the aqueous phase was extracted three times with 25 ml of ethyl acetate. The combined organic phases were dried over magnesium sulphate and filtered, and the solvent was removed under reduced pressure. The residue was purified by flash chromatography (40 g silica cartridge, 40 ml/min, cyclohexane/ethyl acetate gradient). Yield: 216 mg (quant.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434690B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-4882fb5d6bcf4bec8323c16481a11e8b |
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| Source note | uspto-grants-2016_09 |
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