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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463442Generated: October 31, 2026

Water → HCID 54362405, compound

https://huagongshe.com/reaction/1463442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantS-(4,6-Dimethylpyrimidin-2-yl) O-(p-methoxybenzyl) thiocarbonateHCID 100623—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 53864128HCID 53864128—
SolventDichloromethaneHCID 6344—
ProductHCID 54362405HCID 5436240585.5%

Reaction Steps

In 80 ml of methylene chloride was dissolved 7.50 g of (3R,5R,6R)-6-amino-3-(3-benzylideneamino-2-oxoimidazolidin-1-yl)-3-diphenylmethyloxycarbonyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane. Thereto was added 5 g of S-p-methoxybenzyloxycarbonyl-4,6-dimethyl-2-mercaptopyrimidine. The mixture was stirred at room temperature for 2 hours. The reaction mixture was mixed with 80 ml of water, and the resulting mixture was adjusted to pH 7.0 with a saturated aqueous sodium hydrogencarbonate solution. The organic layer was separated, washed with water and a saturated aqueous sodium chloride solution in this order, and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue was purified by column chromatography (eluant: chloroform/acetone=1/0 to 25/1) to obtain 8.36 g (yield: 85.2%) of (3R,5R,6R)-3-(3-benzylideneamino-2-oxoimidazolidin-1-yl)-3-diphenylmethyloxycarbonyl-6-(p-methoxybenzyloxycarbonylamino)-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05300497
Source datasetuspto-grants-1994_04
ORD IDord-9236803c568e4937825fb512d74f3019
Source noteuspto-grants-1994_04