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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndole-3-Acetic AcidHCID 802—
ReactantTriethylamineHCID 8471—
Reactant2-Chloro-1-methylpyridinium iodideHCID 167069—
ReactantHCID 54243495HCID 54243495—
SolventDichloromethaneHCID 6344—
ProductHCID 53747193HCID 5374719382.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05883098
Source datasetuspto-grants-1999_03
ORD IDord-e6069c690a674719b94af10b45fe3199
Source noteuspto-grants-1999_03