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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768025Generated: October 25, 2026

Dimethyl Sulfoxide → 3-{1-(2-naphtho[1,2-b]furan-3-yl-ethyl)-1,2,3,6-tetrahydro-4-pyridinyl}-1H-indole

https://huagongshe.com/reaction/1768025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantDiisopropylethylamineHCID 81531—
Reactant(1,2,3,6-tetrahydro-4-pyridinyl)-1H-indoleHCID 23001082—
Reactant3-(2-Iodo-ethyl)-naphtho[1,2-b]furanHCID 23614451—
Product3-{1-(2-naphtho[1,2-b]furan-3-yl-ethyl)-1,2,3,6-tetrahydro-4-pyridinyl}-1H-indoleHCID 23614450—

Reaction Steps

A mixture of 3-(2-iodo-ethyl)-naphtho[1,2-b]furan (321 mg. 1 mmol) (obtained by the above mentioned process) and 3 (1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole (198 mg, 1 mmol) was heated at 120° C. in DMSO in the presence of N,N-diisopropylethylamine (5 ml, excess) for 24 hrs. At the end, the reaction mixture was quenched with water and extracted with chloroform. The organic layer was washed with water and dried over anhydrous MgSO4 and concentrated to dryness. The dark colored solid was purified by silica-gel column chromatography by eluting it with 70% ethyl acetate:hexane. 3-{1-(2-naphtho[1,2-b]furan-3-yl-ethyl)-1,2,3,6-tetrahydro-4-pyridinyl}-1H-indole was isolated as yellow solid. Yield: 120 mg (30%); 393 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235569B2
Source datasetuspto-grants-2007_06
ORD IDord-71d34400063241b78d77037b8deec5e5
Source noteuspto-grants-2007_06