Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440269Generated: November 2, 2026

Sodium borohydride → HCID 22903503, compound

https://huagongshe.com/reaction/1440269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22903493HCID 22903493—
ReactantMonomethylamine methanolHCID 57454252—
SolventMethanolHCID 887—
ProductHCID 22903503HCID 22903503—

Reaction Steps

To a suspension of 7-chloro-5-oxo-1-[5-(2-methylbenzoylamino)thenoyl]-2,3,4,5-tetrahydro-1H-benzazepine (1 g) in methanol (40 ml) are added molecular sieve 4A (2 g) and 40% methylamine methanol solution (10 ml), and the mixture is refluxed for 6 hours, and cooled. To the mixture is added with stirring sodium borohydride (0.13 g) at room temperature, and the mixture is stirred at the same temperature overnight. The reaction solution is filtered on Celite, and to the filtrate is added water, and the mixture is extracted with dichloromethane. The extract is washed with water, dried over magnesium sulfate, and evaporated under reduced pressure to remove the solvent. The residue is purified by silica gel column chromatography, and recrystallized from dichloromethane-diethyl ether to give 7-chloro-5-methylamino-1-[5-(2-methylbenzoylamino)thenoyl]-2,3,4,5-tetrahydro-1H-benzazepine (0.93 g) as white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05498609
Source datasetuspto-grants-1996_03
ORD IDord-6eedbfe1a9d148b093b4d786433011d6
Source noteuspto-grants-1996_03