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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 750248Generated: October 31, 2026

Methanol → 2-benzyl-6-chloro-4-(4-hydroxymethylphenyl)-1-oxo-1,2-dihydroisoquinoline-3-carboxylic Acid Methyl Ester

https://huagongshe.com/reaction/750248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
Reactant2-benzyl-6-chloro-4-(4-formylphenyl)-1-oxo-1,2-dihydroisoquinoline-3-carboxylic Acid Methyl EsterHCID 86599558—
SolventTetrahydrofuranHCID 8028—
Product2-benzyl-6-chloro-4-(4-hydroxymethylphenyl)-1-oxo-1,2-dihydroisoquinoline-3-carboxylic Acid Methyl EsterHCID 6915657945.2%

Reaction Steps

To a mixture of 2-benzyl-6-chloro-4-(4-formylphenyl)-1-oxo-1,2-dihydroisoquinoline-3-carboxylic acid methyl ester (66 mg), methanol (1.0 ml) and THF (1.0 ml) was added sodium borohydride (6 mg) at 0° C. with stirring, and the mixture was stirred for 1 hr. The reaction mixture was concentrated, and the residue was partitioned between 1N hydrochloric acid and ethyl acetate. The organic layer was dried over magnesium sulfate and concentrated. The residue was purified by preparative HPLC to give the title compound (30 mg) as a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07402595B2
Source datasetuspto-grants-2008_07
ORD IDord-47b997940c734a09a5b6a568e49d6bd6
Source noteuspto-grants-2008_07