Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612293Generated: October 27, 2026

Potassium Carbonate → 4-Methoxybenzyl (6R,7R)-7-Amino-3-((R)-tetrahydrofuran-2-yl)ceph-3-em-4-carboxylate

https://huagongshe.com/reaction/612293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant2-Bromo-1-[(2R)-tetrahydro-2-furanyl]-ethanoneHCID 11194867—
Reactant4-Methoxybenzyl (RS)-2-hydroxy-2-[(lR,5R)-3-benzyl-4-thia-2,6-diazabicyclo[3.2.0)hept-2-en-7-on-6-yl]acetateHCID 53656123—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product4-Methoxybenzyl (6R,7R)-7-Amino-3-((R)-tetrahydrofuran-2-yl)ceph-3-em-4-carboxylateHCID 53841027—

Reaction Steps

4-Methoxybenzyl (RS)-2-hydroxy-2-[(lR,5R)-3-benzyl-4-thia-2,6-diazabicyclo[3.2.0]hept-2-en-7-on-6-yl]acetate (4.103 g) in dichloromethane (15ml) and acetone (15 ml) was ring opened with 4-toluenesulphonic acid hydrate (3.33 g) in water (8 ml) and coupled to (R)-2-bromoacetyltetrahydrofuran (2.11 g) in acetone (20 ml) with potassium carbonate (0.687 g) as described in Example 6(b) for the diastereoisomeric mixture. After purification by flash chromatography, the title compound was obtained as a yellow gum (2.618 g, 49%); [α]D -10.7 (c 1.00 CHCl3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06001997
Source datasetuspto-grants-1999_12
ORD IDord-a75800fa0b72465688fa041da2465320
Source noteuspto-grants-1999_12