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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007025Generated: November 1, 2026

Sodium borohydride → HCID 22502479, compound

https://huagongshe.com/reaction/1007025

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 lSmin. 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 numberUS06790844B2
Source datasetuspto-grants-2004_09
ORD IDord-b4cc1d8bdbf04820a81b3dc6ce8dd14f
Source noteuspto-grants-2004_09