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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034505Generated: November 3, 2026

Sodium Hydroxide → HCID 57183904, compound

https://huagongshe.com/reaction/1034505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 57262936HCID 57262936—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 57183904HCID 5718390489%

Reaction Steps

To a solution of (2S,4S)-1-p-methoxybenzyloxycarbonyl-4-acetylthio-2-sulfamoylaminomethylpyrrolidine (982 mg: 2.35 mmole) in a mixture of dichloromethane (2 ml) and methanol (10 ml), 1N-sodium hydroxide (2.8 ml) is added under ice cooling. The mixture is stirred for 15 minutes. The reaction mixture is diluted with water and extracted with ethyl acetate. The extract is successively washed with water and brine, dried over magnesium sulfate, and concentrated in vacuo. The residue is purified by silica gel column chromatography (toluene:ethyl acetate=1:2) to give (2S,4S)-1-p-methoxybenzyloxycarbonyl-4-mercapto-2-sulfamoylaminomethylpyrrolidine (783 mg). Yield: 89%. NMR δ(CDCl3) ppm: 1.6 to 2.0(m, 2H), 2.4 to 2.7(m, 1H), 3.1 to 3.8(m, 4H), 3.81(s, 3H), 3.9 to 4.2(m, 2H), 4.6 to 5.0(m, 2H), 5.04(s, 2H), 5.97(br s, 1H), 6.89(d, J=8.6 Hz, 2H), 7.30(d, J=8.6 Hz, 2H). IR ν (CHCl3) cm-1 : 3668, 3424, 1683.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05317016
Source datasetuspto-grants-1994_05
ORD IDord-ca267d67158f41459427859363a9d7dd
Source noteuspto-grants-1994_05