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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441256Generated: October 29, 2026

Sodium borohydride → HCID 22405265, compound

https://huagongshe.com/reaction/441256

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22405232HCID 22405232—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductHCID 22405265HCID 2240526593.2%

Reaction Steps

To a solution of 1-{4-[2-(2-methylphenyl)benzoylamino]benzoyl}-2,3,4,5-tetrahydro-1H-1-benzazepin-5-one (620 mg) in methanol (20 ml) was added sodium borohydride (49.4 mg) and the mixture was stirred at ambient temperature for 4 hours. The mixture was diluted with chloroform and the solution was washed with water and brine, and dried over magnesium sulfate. The solvent was evaporated in vacuo to give a syrup and the residue was purified by silica gel column (30g, 1% methanol in chloroform) to give 5-hydroxy-1-{4-[2-(2-methylphenyl)benzoylamino]benzoyl}-2,3,4,5-tetrahydro-1H-1-benzazepine (580 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521170
Source datasetuspto-grants-1996_05
ORD IDord-a5a81026f3d64c4da1ee21ab9ffd8dee
Source noteuspto-grants-1996_05