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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850500Generated: November 2, 2026

Hydrochloric Acid → HCID 19363523, compound

https://huagongshe.com/reaction/850500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 19363399HCID 19363399—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 19363523HCID 1936352347.1%

Reaction Steps

2-(2-Hydroxyethyl)-4-methoxy-3-pentyloxy-N-(2-pyridin-4-ylethyl)-benzamide (90 mg, 233 mmol, 1.0 eq) was dissolved in DMSO (2 ml), and triethylamine (0.3 ml, 2.10 mmol, 9 eq) and sulfur trioxide-pyridine complex (111.2 mg, 0.70 mmol, 3 eq) were successively added under ice-cooling. The mixture was stirred at room temperature for 4 hours. 3N Hydrochloric acid (15 ml) was added to this reaction mixture, and the mixture was stirred at room temperature for 1 hour. Sodium hydroxide was added to make the same alkaline. The solution was extracted twice with ethyl acetate (20 ml). The organic layers were combined, washed with saturated brine (40 ml) and dried over anhydrous sodium sulfate. The drying agent was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by column chromatography on silica gel (ethyl acetate) and recrystallized from ethyl acetate to give 2-[2-(4-pyridyl)ethyl]-methoxy-5-pentyloxy-2H-isoquinolin-1-one (40.2 mg, 47.1%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06017919
Source datasetuspto-grants-2000_01
ORD IDord-bb8638b5fbb0417e8448b3c0ff53e92c
Source noteuspto-grants-2000_01