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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,4-Dimethoxybenzoyl chloride | HCID 2734719 | — |
| Reactant | 1-Piperidin-4-yl-1,3-dihydro-2H-indol-2-one | HCID 2761152 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1-(1-(2,4-Dimethoxybenzoyl)-4-piperidyl)indol-2-one | HCID 22914657 | 45.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05665719 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-75a0481253b94f3ea3f76576417ad1fe |
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| Source note | uspto-grants-1997_09 |
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