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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797619Generated: November 3, 2026

Hydrochloric Acid → HCID 22175226, compound

https://huagongshe.com/reaction/1797619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantOxalyl chlorideHCID 65578—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22175966HCID 22175966—
CatalystDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 22175226HCID 2217522679.5%

Reaction Steps

To a mixed solution of 6-benzyloxy-2-isobutyl-4-(4-methylphenyl)-1-oxo-1,2-dihydro-3-isoquinolinecarboxylic acid (5.74 g, 13 mmol) in tetrahydrofuran (50 ml) were added oxalyl chloride (1.4 ml, 15.6 mmol) and N,N-dimethylformamide (3 drops), and the mixture was stirred at room temperature for 1 h. The reaction mixture was concentrated under reduced pressure and the residue was dissolved in tetrahydrofuran (20 ml) The obtained solution was added dropwise to a suspension of sodium tetrahydroborate (1.72 g, 45.5 mmol) in 1,2-dimethoxyethane (50 ml) at 0° C. The obtained mixture was stirred at 0° C. for 1 h. The reaction mixture was poured into 1N hydrochloric acid and extracted with ethyl acetate. The extract was washed with brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The obtained crystals were recrystallized from ethyl acetate-diisopropyl ether to give 6-benzyloxy-3-hydroxymethyl-2-isobutyl-4-(4-methylphenyl)-1-(2H)-isoquinolinone (4.41 g, 79.5%) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07034039B2
Source datasetuspto-grants-2006_04
ORD IDord-5db190ad8c5144cca75dfae269d539c5
Source noteuspto-grants-2006_04