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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699538Generated: October 31, 2026

Tetrahydrofuran → HCID 131723117, compound

https://huagongshe.com/reaction/1699538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactantallyl (1S,5R,6S)-2-(hydroxymethyl)-6-[1(R)-allyloxycarbonyloxy-ethyl]-1-methylcarbapen-2-em-3-carboxylateHCID 11046746—
ReactantHCID 18319501HCID 18319501—
SolventChloroformHCID 6212—
ProductHCID 131723117HCID 131723117—

Reaction Steps

A solution of allyl (1S,5R,6S)-6-[1(R)-allyloxycarbonyloxy-ethyl]-2-hydroxymethyl-1-methyl-carbapen-2-em-3-carboxylate (365 mg, 1.0 mmol), triphenylphosphine (315 mg, 1.2 mmol), and 4-phenyl-6-(2-triethylsilanyloxy-ethyl)-2H-1-thia-2,3-diaza-naphthalene 1,1-dioxide (458mg, 1.1 mmol) in anhydrous tetrahydrofuran (7 mL) is cooled in an ice-bath and stirred under a nitrogen atmosphere while diisopropyl azodicarboxylate (0.24 mL, 1.2 mmol) is added dropwise over a few minutes. The resulting solution is stirred in the cold for 30 minutes, then diluted with chloroform, washed with 5% aqueous sodium bicarbonate and brine, dried over sodium sulfate, filtered and evaporated under vacuum. The residue is purified by silica gel flash chromatography, eluting with hexane-ethyl acetate, to afford allyl (1S,5R,6S)-6-[(1(R)-allyloxycarbonyloxy-ethyl]-2-[1,1-dioxo-4-phenyl-6-(2-triethylsilanyloxy-ethyl)-2H-1-thia-2,3-diaza-naphthalen-2-ylmethyl]-1-methyl-carbapen-2-em-3-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06346525B1
Source datasetuspto-grants-2002_02
ORD IDord-a8838effeba74502b60c99e37ec31342
Source noteuspto-grants-2002_02