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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199492Generated: November 3, 2026

1,1'-Carbonyldiimidazole → 1,8-Diazabicyclo(5.4.0)undec-7-ene

https://huagongshe.com/reaction/1199492

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 12602969HCID 12602969—
SolventDimethylformamideHCID 6228—
Product1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—

Reaction Conditions

Temperature40 °C

Reaction Steps

2.925 g (0.0075 mol) of (R)-N-(ethoxymethyl)-1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3-methoxycarbonylpyridine-5-carboxylic acid and 1.34 g (0.0082 mol) of carbonyldiimidazole are dissolved in 50 ml of dimethylformamide. The mixture is heated at 40° C. for one hour. 2.13 g (0.0075 mol) of the product obtained in Preparation XX and 1.12 ml (0.0075 mol) of 1,8-diazabicyclo[5.4.0]undec-7-ene are then added to the reaction medium. The mixture is heated to 100° C. After 2 hours, the mixture is left to cool and then poured into 100 ml of water. The medium is extracted 3 times with 30 ml of ethyl acetate. The organic phases obtained are washed twice with 10 ml of water, dried over magnesium sulfate and filtered and the solvent is evaporated off. The crude product obtained is purified by flash chromatography, elution being carried out with a toluene/isopropanol mixture (97:3 v/v). This gives 4.8 g (yield: 98%) of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04900833
Source datasetuspto-grants-1990_02
ORD IDord-5dd615237fcc49d78a41b292c39494f6
Source noteuspto-grants-1990_02