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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33231Generated: October 29, 2026

Sodium triacetoxyborohydride → HCID 69311958, compound

https://huagongshe.com/reaction/33231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 69181179HCID 69181179—
Reactant4-(4-Methyl-5-quinolin-6-yl-4H-[1,2,4]triazol-3-ylsulfanyl)-butyraldehydeHCID 86594173—
SolventDichloromethaneHCID 6344—
ProductHCID 69311958HCID 6931195821%

Reaction Steps

4-(4-Methyl-5-quinolin-6-yl-4H-[1,2,4]triazol-3-ylsulfanyl)-butyraldehyde (0.1 g, 0.32 mmol) and 7-Ethanesulfonyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine (0.11 g, 0.45 mmol) were stirred at room temperature in dichloromethane (4 ml) for 20 min. Sodium triacetoxyborohydride (71 mg, 0.34 mmol) was then added and the mixture stirred overnight. The mixture was diluted with dichloromethane (50 ml) and washed with saturated sodium bicarbonate solution (30 ml). The aqueous was extracted with further dichloromethane (50 ml) and the combined organic portions were dried (Na2SO4), filtered and evaporated to give a yellow oil. Purification by silica gel chromatography (eluent 10% MeOH:EtOAc) which gave the title compound as a colourless oil (35 mg, 21%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429579B2
Source datasetuspto-grants-2008_09
ORD IDord-f6b7a8833b22409d8684a62ec3804fae
Source noteuspto-grants-2008_09