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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 233944Generated: October 26, 2026

N-methyl-2-pyrrolidone → 1-(4-(3-(4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl)propoxy)-3-methoxyphenyl)-2-hydroxyethanone

https://huagongshe.com/reaction/233944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazoleHCID 849421—
Reactant4-(3-Chloropropoxy)-3-methoxyphenyl-2-hydroxyethanoneHCID 18467332—
SolventWaterHCID 962—
Product1-(4-(3-(4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl)propoxy)-3-methoxyphenyl)-2-hydroxyethanoneHCID 18467218—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 3-(4-piperidinyl)-6-fluoro-1,2-benzisoxazole (1.3 g, 5.8 mmol), 1-[4-(3-chloropropoxy)-3-methoxyphenyl]-2-hydroxyethanone (1.5 g, 5.8 mmol), NaHCO3 (1.5 g) and 1-methyl-2-pyrrolidinone (50 ml) was stirred under N2 at 100° C. for 6 hours. The reaction was poured into H2O, and the aqueous suspension was extracted with EtOAc. The extract was washed (H)), dried (MgSO4) and concentrated to afford the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05593995
Source datasetuspto-grants-1997_01
ORD IDord-c3b5648f52fe4934bedcffad53e3faa4
Source noteuspto-grants-1997_01