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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814583Generated: October 31, 2026

Sodium borohydride → HCID 22502479, compound

https://huagongshe.com/reaction/1814583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 20720265HCID 20720265—
SolventMethanolHCID 887—
ProductHCID 22502479HCID 2250247959.7%

Reaction Steps

1-(4-Ethylpiperazin-1-yl)-3-(1-indanon-5-yl)isoquinoline (0.20 g) obtained in the previous Example was dissolved in methanol (20 ml), followed by the addition of sodium borohydride (0.10 g) at room temperature, and the mixture was reacted for 15 min. The reaction solution was concentrated, and the resulting residue was partitioned between ethyl acetate and water. The ethyl acetate layer was separated, washed with water and brine, and dried over magnesium sulfate. The solvent was evaporated, and the resulting residue was purified by silica gel column chromatography (methylene chloride/methanol system), to give the title compound (0.12 g) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875761B2
Source datasetuspto-grants-2005_04
ORD IDord-0eddda3442d5499a97713355968269d9
Source noteuspto-grants-2005_04