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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955845Generated: October 30, 2026

Dimethylformamide → 1-[4-[2-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)1-piperidinyl]ethoxy]-3-methoxyphenyl]ethanone

https://huagongshe.com/reaction/1955845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantR-56109 hydrochlorideHCID 11334359—
Reactant1-[4-(2-Chloroethoxy)-3-methoxyphenyl]ethanoneHCID 14407170—
SolventWaterHCID 962—
Product1-[4-[2-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)1-piperidinyl]ethoxy]-3-methoxyphenyl]ethanoneHCID 1043181248.5%

Reaction Steps

A stirred mixture of 6-fluoro-3(4-piperidinyl)-1,2 benzisoxazole hydrochloride (5.1 g, 20 mmol), K2CO3 (5.2 g), 1-[4-(2chloroethoxy)-3-methoxyphenyl]ethanone (5.0 g, 1022 mmol), and dimethylformamide (90 ml) was heated at 90 f° C. or 16 hours. The reaction was poured into water, and the aqueous mixture was extracted with ethyl acetate. The ethyl acetate was washed (water), dried (MgSO4) and concentrated to afford 7.4 of a yellow solid. The solid was chromatographed on a Waters Prep LC 500 utilizing dichloromethane/methanol (4%) as eluent, and subsequent concentration of the appropriate fraction afforded 4.0 g of a yellow solid. The solid was recrystallized from ethyl alcohol to yield 3.1 g (38%) of 1-[4-[2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperindyl]ethoxy]-3-methoxyphenyl]ethanone, as slightly yellow flakes, m.p.=132°-134° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05776963
Source datasetuspto-grants-1998_07
ORD IDord-e16e380fd3eb45859af041e8100c5ab5
Source noteuspto-grants-1998_07