HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418566Generated: November 2, 2026
Indole-3-Acetic Acid → HCID 53747193, compound
https://huagongshe.com/reaction/1418566
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Indole-3-Acetic Acid | HCID 802 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chloro-1-methylpyridinium iodide | HCID 167069 | — |
| Reactant | HCID 54243495 | HCID 54243495 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53747193 | HCID 53747193 | 82.3% |
Reaction Steps
To a stirred mixture of (2R)-2-benzyl-1-[3,5-bis(trifluoromethyl)benzoyl]piperazine (0.3 g) and 2-(1H-indol-3-yl)acetic acid (0.13 g) in dichloromethane (8 ml) containing triethylamine (0.25 ml) was added 2-chloro-1-methylpyridinium iodide (0.22 g) at room temperature under nitrogen atmosphere. After being stirred for 5 hours, the reaction mixture was diluted with dichloromethane and washed with 0.1N hydrochloric acid, aqueous saturated sodium bicarbonate solution and brine, and dried over magnesium sulfate. After removal of the solvent, the residue was purified by column chromatography on silica gel using chloroform-methanol (50:1) as eluent to give (2R)-2-benzyl-1-[3,5-bis(trifluoromethyl)benzoyl]-4-[2-(1H-indol-3-yl)acetyl]piperazine (0.34 g) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05883098 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-e6069c690a674719b94af10b45fe3199 |
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| Source note | uspto-grants-1999_03 |
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