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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586746Generated: October 31, 2026

Thioacetic acid → HCID 57260090, compound

https://huagongshe.com/reaction/1586746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioacetic acidHCID 10484—
ReactantSodium hydrideHCID 24758—
ReactantHCID 57141099HCID 57141099—
SolventDimethylformamideHCID 6228—
ProductHCID 57260090HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05215983
Source datasetuspto-grants-1993_06
ORD IDord-e2f1f7732fad497f8738420403cccaf4
Source noteuspto-grants-1993_06