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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698766Generated: November 1, 2026

2-oxo-3-tert-butoxycarbonylamino-5-(2-cyclohexen-1-yl)-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine → 2-Oxo-3-tert-butoxycarbonylamino-5-cyclohexyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine

https://huagongshe.com/reaction/1698766

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-oxo-3-tert-butoxycarbonylamino-5-(2-cyclohexen-1-yl)-1,3,4,5-tetrahydro-2H-1,5-benzodiazepineHCID 15490832—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
Product2-Oxo-3-tert-butoxycarbonylamino-5-cyclohexyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepineHCID 1549083374%

Reaction Steps

To a solution of (±)-2-oxo-3-tert-butoxycarbonylamino-5-(2-cyclohexen-1-yl)-1,3,4,5-tetrahydro-2H-1,5-benzo diazepine (4.5 g) in ethanol (200 mL), 10% palladium carbon (1 g) was added, followed by stirring at room temperature for 2 hours under a hydrogen atmosphere. The reaction mixture was filtered, and the filtrate was concentrated under the reduced pressure. The residue was then recrystallized from ethanol, whereby the title compound (3.35 g) was obtained. Yield: 74%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06344452B1
Source datasetuspto-grants-2002_02
ORD IDord-d78f9b4bab644460a9f14f0126e47760
Source noteuspto-grants-2002_02