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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1679924Generated: November 1, 2026

2-(m-Nitrophenyl)-3,4-diazabicyclo[4.1.0]hept-2-en-5-one → HCID 23458522, compound

https://huagongshe.com/reaction/1679924

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(m-Nitrophenyl)-3,4-diazabicyclo[4.1.0]hept-2-en-5-oneHCID 23458511—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23458522HCID 2345852269%

Reaction Steps

1.5 g (6.5 millimoles) of 2-(m-nitrophenyl)-3,4-diaza-bicyclo[4.1.0]hept-2-en-5-one (see Example 32b), dissolved in 80 ml of tetrahydrofuran, are hydrogenated with 0.5 g of 10% strength palladium on charcoal at room temperature. When the hydrogen absorption has ceased, the catalyst is filtered off and the filtrate is concentrated. The residue is recrystallized from an ethyl acetate/methanol mixture. 0.9 g (69% of theory) of 2-(m-aminophenyl)-3,4-diaza-bicyclo[4.1.0]hept-2-en-5-one is obtained as colorless crystals, which are identical with the compound from Example 33.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04271163
Source datasetuspto-grants-1981_06
ORD IDord-5af43b8c4c4e406e9d64055ff8542ed9
Source noteuspto-grants-1981_06