Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thioacetic acid | HCID 10484 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 57141099 | HCID 57141099 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57260090 | HCID 57260090 | — |
Reaction Steps
To a solution of sodium hydride (60% suspension in oil, 0.27 g) in N,N-dimethylformamide (15 ml) was added dropwise thioacetic S-acid (0.51 ml) with stirring under ice-cooling. The mixture was stirred at the same temperature for 30 minutes. A solution of (2S,4R)-4-methanesulfonyloxy -1-(4-nitrobenzyloxycarbonyl)-2-{4,5,6,7-tetrahydropyrazolo [1,5-a]pyrimidin-4-yl)methylpyrrolidine (2.65 g) in N,N-dimethylformamide (15 ml) was added to the mixture obtained above with stirring at the same temperature and the mixture was stirred at 80°~90° C. for 2 hours. The reaction mixture was poured into ice-water (100 ml) and extracted twice with ethyl acetate (100 ml). The extract was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and evaporated in vacuo. The resulting residue was chromatographed on silica gel (150 g) eluting with a mixture of chloroform and methanol (19:1, V/V). The fractions containing the desired compound were collected and evaporated in vacuo to give (2S,4S)-4-acetylthio-1-(4-nitrobenzyloxycarbonyl) -2-{4,5,6,7-tetrahydropyrazolo-[1,5-a]pyrimidin-4-yl}methylpyrrolidine (2.23 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05215983 |
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| Source dataset | uspto-grants-1993_06 |
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| ORD ID | ord-e2f1f7732fad497f8738420403cccaf4 |
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| Source note | uspto-grants-1993_06 |
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