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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377688Generated: October 25, 2026

Triethylamine → 1-(1-(2,4-Dimethoxybenzoyl)-4-piperidyl)indol-2-one

https://huagongshe.com/reaction/1377688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,4-Dimethoxybenzoyl chlorideHCID 2734719—
Reactant1-Piperidin-4-yl-1,3-dihydro-2H-indol-2-oneHCID 2761152—
SolventChloroformHCID 6212—
Product1-(1-(2,4-Dimethoxybenzoyl)-4-piperidyl)indol-2-oneHCID 2291465745.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

1-(4-Piperidyl)indol-2-one (53 mg, 0.245 mmole), 2,4-dimethoxybenzoyl chloride (54 mg, 0.27 mmole), and 38 mL (0.27 mmole) triethylamine were mixed in 4 ml of chloroform at 0° C. The reaction mixture was stirred at 0° C. for 5 minutes and then at 23° C. for 15 minutes during which time the pH was adjusted to 7.5 with triethylamine. The reaction mixture was concentrated under reduced pressure and the residue was purified by preparative thick layer chromatography (CHCl3 --CH3OH--NH4OH; 95:5:0.5) to yield 42 mg of the title compound: m.p. 88°-93° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665719
Source datasetuspto-grants-1997_09
ORD IDord-75a0481253b94f3ea3f76576417ad1fe
Source noteuspto-grants-1997_09