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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797594Generated: November 3, 2026

Hydrochloric Acid → HCID 22175926, compound

https://huagongshe.com/reaction/1797594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantOxalyl chlorideHCID 65578—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22175177HCID 22175177—
CatalystDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 22175926HCID 2217592690.2%

Reaction Steps

To a solution of 6-benzyloxy-4-(4-fluorophenyl)-2-isobutyl-1-oxo-1,2-dihydro-3-isoquinolinecarboxylic acid (3.79 g, 8.5 mmol) in tetrahydrofuran (30 mL) were added oxalyl chloride (0.9 mL, 10.2 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 (1.13 g, 30 mmol) in 1,2-dimethoxyethane (30 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 residue was purified by silica gel column chromatography to give 6-benzyloxy-4-(4-fluorophenyl)-3-hydroxymethyl-2-isobutyl-1(2H)-isoquinolinone (3.31 g, 90.2%) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07034039B2
Source datasetuspto-grants-2006_04
ORD IDord-05b8aef7bfeb422f983537c1b2a1b728
Source noteuspto-grants-2006_04