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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402535Generated: October 26, 2026

Water → 2-(4-Methoxy-benzyl)-6-((1S,3S)-3-amino-cyclopentyloxy)-2H-isoquinolin-1-one

https://huagongshe.com/reaction/402535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant(1S,3S)-3-Aminocyclopentan-1-olHCID 42614395—
Reactant6-Fluoro-2-[(4-methoxyphenyl)methyl]isoquinolin-1-oneHCID 59818260—
SolventDimethylacetamideHCID 31374—
Product2-(4-Methoxy-benzyl)-6-((1S,3S)-3-amino-cyclopentyloxy)-2H-isoquinolin-1-oneHCID 5922483949%

Reaction Conditions

Temperature80 °C

Reaction Steps

106 mg (4.20 mmol) of sodium hydride (95%) were suspended in 3 mL of dimethyl acetamide and 193 mg (1.40 mmol) of (1S,3S)-3-amino-cyclopentanol (34), dissolved in 1 mL of dimethyl acetamide, were added dropwise. After 1 h, 402 mg (1.42 mmol) of 2-(4-methoxy-benzyl)-6-fluoro-2H-isoquinolin-1-one (9), dissolved in another 3 mL of dimethyl acetamide, were added. The reaction mixture was stirred at 80° C. until the reaction was complete. The mixture was poured into water, extracted three times with a mixture of dichloromethane and 2-propanol (3:1) and the combined organic layers were evaporated. Water was added and the crude product was subjected to lyophilization to remove remainders of dimethyl acetamide. The obtained crude product was purified by silica gel chromatography to yield 250 mg of the title compound (39). Rt=1.20 min (Method E). Detected mass: 365.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742116B2
Source datasetuspto-grants-2014_06
ORD IDord-781560f9d9294b6b808b054dca68a86f
Source noteuspto-grants-2014_06