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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223265Generated: October 30, 2026

Dimethylformamide → 3-(4-[5,6-Dimethoxy-1,2-benzisoxazol-3-yl]piperidyl}-2-methyl indole

https://huagongshe.com/reaction/223265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant5,6-Dimethoxy-3-(4-piperidyl)-1,2-benzisoxazoleHCID 13076426—
Reactant2-Methyl-3-(phenylsulfonylpropyl)indoleHCID 13450900—
SolventWaterHCID 962—
Product3-(4-[5,6-Dimethoxy-1,2-benzisoxazol-3-yl]piperidyl}-2-methyl indoleHCID 8673858726.8%

Reaction Steps

A stirred mixture of 5.0 g of 5,6-dimethoxy-3-(4-piperidyl)-1,2-benzisoxazole, 6.78 g of 2-methyl-3-(phenylsulfonylpropyl)indole, 120 ml of dimethylformamide and 15.0 g of anhydrous potassium carbonate was heated to 90° for 6 hrs and overnight at ambient temperature. The mixture was poured into water (300 ml) and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and the solvent was removed in vacuo to yield a solid. The solid was purified by passing it through a silica gel column (20:1) and eluting it with dichloromethane-methanol (1%). Recrystallization two times from ethanol-water yielded 2.0 g (24%) of product, mp 176°-178°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04352811
Source datasetuspto-grants-1982_10
ORD IDord-11c789af77164c3e95c1fe0087bc6bf8
Source noteuspto-grants-1982_10