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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420272Generated: November 1, 2026

HCID 131729363, compound → HCID 131729362, compound

https://huagongshe.com/reaction/420272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131729363HCID 131729363—
CatalystZincchlorideHCID 3007855—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
SolventPotassium CarbonateHCID 11430—
ProductHCID 131729362HCID 131729362—

Reaction Steps

To a solution of N′-[4-[(3aR*,7S*,7aS*)-3-(3-tert-butyl-benzyl)-2,5,5-trioxo-octahydro-1-oxa-5lambda*6*-thia-3-aza-inden-7-ylmethyl]-2-fluoro-6-((S)-3,3,3-trifluoro-2-hydroxy-propyl)-phenyl]-N,N-dimethyl-formamidine (0.11 g, 0.17 mmol) in anhydrous EtOH (3 mL) was added ZnCl2 (0.12 g, 0.86 mmol) and the reaction mixture was heated at reflux for 8 h. The reaction mixture was diluted with EtOAc and aq. K2CO3 solution. The product was extracted with EtOAc and the combined organic layers were washed with brine, dried over MgSO4, filtered and evaporated. The crude product was purified by flash-chromatography on silica gel (hexane-EtOAc 2:1 to 1:2) to yield the title compound as a colorless foam: TLC (hexane-EtOAc 1:1) Rf=0.39; HPLC RtA=2.21 min; ESIMS [M+H]+=573.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093406B2
Source datasetuspto-grants-2012_01
ORD IDord-1a6eceb668be4a27946635e457efe9a1
Source noteuspto-grants-2012_01