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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797473Generated: November 2, 2026

Hydrochloric Acid → HCID 22176368, compound

https://huagongshe.com/reaction/1797473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantOxalyl chlorideHCID 65578—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22175425HCID 22175425—
CatalystDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 22176368HCID 2217636866.7%

Reaction Steps

6-Chloro-4-methoxy-2-methyl-1-oxo-1,2-dihydro-3-isoquinolinecarboxylic acid (0.67 g, 2.5 mmol) was dissolved in tetrahydrofuran (10 ml) and oxalyl chloride (0.26 ml, 3 mmol) and N,N-dimethylformamide (2 drops) were added thereto. 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 (10 ml). The obtained solution was added dropwise to a suspension of sodium tetrahydroborate (0.33 g, 8.8 mmol) in 1,2-dimethoxyethane (20 ml) at 0° C. The obtained mixture was stirred at 0° C. for 1 h, and 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-chloro-3-hydroxymethyl-4-methoxy-2-methyl-1(2H)-isoquinolinone (0.42 g, 66.7%) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07034039B2
Source datasetuspto-grants-2006_04
ORD IDord-0f3d8914d6714672ab97b98ec88f6056
Source noteuspto-grants-2006_04