Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979415Generated: October 25, 2026

Water → 2-oxo-3-tert-butoxycarbonylamino-5-(furan-2-ylcarbonyl)-8-methyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine

https://huagongshe.com/reaction/1979415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
Reactant2-Furancarbonyl chlorideHCID 68242—
Reactant2-oxo-3-tert-butoxycarbonylamino-8-methyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepineHCID 21201581—
Solvent1,2-DichloroethaneHCID 11—
Product2-oxo-3-tert-butoxycarbonylamino-5-(furan-2-ylcarbonyl)-8-methyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepineHCID 2120186781.3%

Reaction Steps

2-Oxo-3-tert-butoxycarbonylamino-8-methyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine (2.00 g) obtained from Referential Example 7 was suspended in 1,2-dichloroethane (40 ml), 2-furancarbonyl chloride (1.05 g) and pyridine (626 mg) were added thereto, the mixture was refluxed for 2 hours. Water (100 ml) was added to the reaction mixture, extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium bicarbonate, dried over anhydrous sodium sulfate, the solvent was evaporated under reduced pressure, and diisopropyl ether was added to the residue for trituration, collected by filtration, to thereby obtain 2.15 g of the titled compound (Yield: 77,4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06239131B1
Source datasetuspto-grants-2001_05
ORD IDord-c562e42d7d3749dba0d177e62d45f0fe
Source noteuspto-grants-2001_05