Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698774Generated: October 31, 2026

Hydrochloric Acid → HCID 53659154, compound

https://huagongshe.com/reaction/1698774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantNitrobenzeneHCID 7416—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 57016129HCID 57016129—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventO-XyleneHCID 7237—
ProductHCID 53659154HCID 5365915460.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of (3R)-2-oxo-3-butoxycarbonylamino-5-(2-cyclohexen-1-yl)-1,3,4,5-tetrahydro-2H-1,5-benzodiazepin e (12.87 g) in xylene (200 mL), nitrobenzene (22.16 g) and 10% palladium carbon (6 g) were added, followed by refluxing for 1 hour and 30 minutes. The reaction mixture was allowed to cool down and then filtered. The filtrate was concentrated under reduced pressure. The residue was dissolved in ethanol (30mL), and a 4 N hydrochloric acid-dioxane solution (20 mL) was added, followed by stirring at 50° C. for 1 hour. After the reaction mixture was allowed to cool down, crystals so precipitated were collected by filtration and washed with 2-propanol, whereby the hydrochloride of the title compound was obtained. The hydrochloride was then dissolved under heat in a mixed solution of methanol and water. After the reaction mixture was allowed to cool down, a saturated aqueous solution of sodium hydrogencarbonate was added to the reaction mixture for neutralization. Crystals so precipitated were collected by filtration, washed with water and then dried, whereby the title compound (5.55 g) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06344452B1
Source datasetuspto-grants-2002_02
ORD IDord-44e994ece9af415c82660891d9940d9f
Source noteuspto-grants-2002_02