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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250843Generated: October 31, 2026

Trifluoroacetic acid → HCID 69979687, compound

https://huagongshe.com/reaction/1250843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1H-Indole-5-Carboxylic AcidHCID 74280—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 18504925HCID 18504925—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 69979687HCID 6997968754%

Reaction Steps

To a solution of 1-BOC-2-methyl-4-benzylpiperidine (0.29 g, 1.0 mMol) in 5 mL of dichloromethane was added trifluoroacetic acid (TFA) (0.5 mL). After stirring at rt for 10 h the reaction mixture was evaporated in vacuo and azeotroped twice with dichloromethane and twice with hexane. The residue was dissolved in 5 mL of dichloromethane and diisopropylethylamine (1.6 mL, 10 mMol) was added. In a separate flask a mixture of 5-indolecarboxylic acid (0.19 g, 1.2 mMol) and EDAC (0.23 g, 1.2 mMol) was dissolved in 15 mL of dichloromethane and stirred at rt for 5 min. To this reaction mixture was added the first solution, and the resulting mixture stirred at rt for 20 h. The reaction mixture was poured into water and extracted with ethyl acetate (2×50 mL). The combined organic extract was washed with water and brine. The extract was dried over NASO4 and evaporated. The residue was chromatographed on a column of silica gel with 1% MeOH-dichloromethane. Evaporation of the desired fractions gave 0.18 g (54%) of the product as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06340685B1
Source datasetuspto-grants-2002_01
ORD IDord-f3421eaed220422984325f273bb2a661
Source noteuspto-grants-2002_01