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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930207Generated: October 27, 2026

Water → 4-[2-(4-Methoxy-benzyl)-7-methyl-1-oxo-1,2-dihydro-isoquinolin-6-yloxy]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1930207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
Reactant6-fluoro-2-(4-methoxybenzyl)-7-methylisoquinolin-1(2H)-oneHCID 59226043—
SolventDimethylacetamideHCID 31374—
Product4-[2-(4-Methoxy-benzyl)-7-methyl-1-oxo-1,2-dihydro-isoquinolin-6-yloxy]-piperidine-1-carboxylic acid tert-butyl esterHCID 6745797488.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 3.2 g (15.9 mmol) 1-tert-butoxycarbonyl-4-hydroxypiperidine in 110 mL dimethylacetamide was stirred with 1.36 g (45.4 mmol) of 80-% sodium hydride for 1 h at room temperature. Then a suspension of 4.5 g (15.1 mmol) of 6-fluoro-2-(4-methoxy-benzyl)-7-methyl-2H-isoquinolin-1-one in dimethylacetamide was added. The reaction mixture was heated to 80° C. for 2 h during which time a clear solution was obtained. The reaction mixture was slowly added to 160 mL water and after 1 h of stirring the product was isolated by filtration and dried over night in vacuum. 6.4 g of 4-[2-(4-Methoxy-benzyl)-7-methyl-1-oxo-1,2-dihydro-isoquinolin-6-yloxy]-piperidine-1-carboxylic acid tert-butyl ester were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188117B2
Source datasetuspto-grants-2012_05
ORD IDord-dd3b2ba9860543f1bb46e5276793c3f4
Source noteuspto-grants-2012_05