HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420272Generated: November 1, 2026
HCID 131729363, compound → HCID 131729362, compound
https://huagongshe.com/reaction/420272
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 131729363 | HCID 131729363 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Potassium Carbonate | HCID 11430 | — |
| Product | HCID 131729362 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093406B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-1a6eceb668be4a27946635e457efe9a1 |
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| Source note | uspto-grants-2012_01 |
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