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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 750247Generated: October 31, 2026

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

https://huagongshe.com/reaction/750247

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-2-buteneHCID 10553—
ReactantSodium ChloriteHCID 23668197—
ReactantMonosodium phosphateHCID 23672064—
Reactant2-benzyl-6-chloro-4-(4-formylphenyl)-1-oxo-1,2-dihydroisoquinoline-3-carboxylic Acid Methyl EsterHCID 86599558—
Solvent1-ButanolHCID 263—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-benzyl-4-(4-carboxyphenyl)-6-chloro-1-oxo-1,2-dihydroisoquinoline-3-carboxylic Acid Methyl EsterHCID 6915647034.2%

Reaction Steps

To a mixture of 2-benzyl-6-chloro-4-(4-formylphenyl)-1-oxo-1,2-dihydroisoquinoline-3-carboxylic acid methyl ester (93 mg), sodium dihydrogenphosphate (26 mg), 2-methyl-2-butene (100 μl), THF (2.0 ml), butanol (1.0 ml) and water (2.0 ml) was added sodium chlorite (73 mg) at 0° C. with stirring, and the mixture was stirred for 1 hr. The solvent was removed 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 (33 mg) as a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07402595B2
Source datasetuspto-grants-2008_07
ORD IDord-e50b868c3f1d436b886a8eefdc5dc53a
Source noteuspto-grants-2008_07