Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (S)-styrene oxide | HCID 114946 | — |
| Reactant | HCID 77776170 | HCID 77776170 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 22466446 | HCID 22466446 | — |
Reaction Steps
A mixture of compound (37) (0.0043 mol) and (S)-phenyl oxirane (0.005 mol) in 2-propanol (50 ml) was stirred and refluxed overnight. (S)-phenyl oxirane (0.005 mol) was added again. The mixture was stirred and refluxed for 3 hours. The solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH 99/1). The pure fractions were collected and the solvent was evaporated. The residue was triturated in DIPE, filtered off and dried, yielding 1.6 g (47%) of [2S-[2α,4α[(S*,R*)(R*)]]]4-[4-[4-[4-[[2-(2,4-difluorophenyl)-2-(1H-1,2,4-triazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]-1-piperazinyl]phenyl]-2,4-dihydro-2-[2[(2-hydroxy-2-phenylethyl)amino]-1-methylpropyl]-3H-1,2,4-triazol-3-one (compound 81).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06384030B1 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-43690f4af3c249dcbdeaa95d4c0f58e5 |
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| Source note | uspto-grants-2002_05 |
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