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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941570Generated: November 3, 2026

Pyridine → HCID 22851803, compound

https://huagongshe.com/reaction/1941570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHCID 22851804HCID 22851804—
CatalystSilver NitrateHCID 24470—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 22851803HCID 2285180383.2%

Reaction Steps

To a solution of (2S,4S)-1-p-methoxybenzyloxycarbonyl-4-tritylthio-2-(N-p-methoxybenzyloxycarbonyl-N-methylaminosulfonyl)aminomethylpyrrolidine (1.5 g: 1.88 mmole) in a mixture of dichloromethane (4 ml) and methanol (10 ml), a solution of pyridine (381 μl: 2.5 eq.) and silver nitrate (640 mg: 2 eq.) in water (6 ml) is added with stirring under ice cooling. The mixture is stirred at the same temperature for 30 minutes. The reaction mixture is diluted with dichloromethane, washed with water, dried over magnesium sulfate, and concentrated in vacuo to about 5 ml. The residue is dissolved in methanol (10 ml) and hydrogen sulfide is bubbled through it. The mixture freed from solid by filtering is concentrated in vacuo. The residue is purified by silica gel column chromatography (toluene: ethyl acetate=2:1) to give (2S,4S)-1-p-methoxybenzyloxycarbonyl-4-mercapto-2-(N-p-methoxybenzyloxycarbonyl-N-methylaminosulfonyl)aminomethylpyrrolidine (866 mg). Yield: 83%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05703243
Source datasetuspto-grants-1997_12
ORD IDord-10b04595ad4c4f25a6bb0b2adc87a0d1
Source noteuspto-grants-1997_12