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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372710Generated: November 4, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 14459722, compound

https://huagongshe.com/reaction/2372710

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 14459667HCID 14459667—
ReactantHCID 131717216HCID 131717216—
SolventDichloromethaneHCID 6344—
ProductHCID 14459722HCID 1445972253.7%

Reaction Steps

1.46 g (6 mmol) of 7-amino-3-methoxymethyl-3-cephem-4-carboxylate were suspended in 30 ml of methylene chloride, and 0.92 ml (6 mmol) of 1,8-diazabicyclo-(5,4,0)-undec-7-ene (DBU) was added at 0° C. After 30 minutes, 1.66 g (6.5 mmol) of iodomethyl 2,2-dimethyl-butyrate (compare preparation example 4) were added, while cooling with ice, and the mixture was subsequently stirred at room temperature for 2 hours. The precipitate which had separated out was filtered off with suction and the crude product was chromatographed (SiO2 ; toluene/ethyl acetate=1:1). 1.2 g (53%) of the title compound were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05100887
Source datasetuspto-grants-1992_03
ORD IDord-18fa53b0b44b4592b0758b085f07879c
Source noteuspto-grants-1992_03