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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402883Generated: October 26, 2026

Trifluoroacetic acid → 2-(6-Dimethylaminomethyl-2-methyl-indolizin-3-yl)-acetamide

https://huagongshe.com/reaction/402883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
Reactant(6-Dimethylaminomethyl-2-methyl-indolizin-3-yl)-acetic acid tert-butyl esterHCID 68712027—
SolventDichloromethaneHCID 6344—
Product2-(6-Dimethylaminomethyl-2-methyl-indolizin-3-yl)-acetamideHCID 5919202191.7%

Reaction Steps

(6-Dimethylaminomethyl-2-methyl-indolizin-3-yl)-acetic acid tert-butyl ester (122 mg, 0.40 mmol) is dissolved in CH2Cl2 (10 ml) containing 5% of trifluoroacetic acid. The mixture is stirred for 14 hours at room temperature and then concentrated in vacuo. The residue is azeotroped twice with toluene, dissolved in N,N-dimethylformamide (2.0 ml) and treated with carbonyl diimidazole (76 mg, 0.44 mmol, 1.1 equiv). After 1 hour at room temperature, the volatiles are removed in vacuo, and the activated acid is taken up in concentrated aqueous ammonia (10 ml). The mixture is stirred for 30 minutes at room temperature and then concentrated in vacuo. The residue is purified via flash chromatography (CH2Cl2/MeOH 7:1) to afford the title compound (90 mg, 91%). 1H NMR (400 MHz, d6-DMSO): δ=7.31 (s, 1H), 7.27 (s, 1H), 6.75 (s, 1H), 6.61 (dd, J=9.3/1.5 Hz, 1H), 4.06 (s, 2H), 3.38 (s, 2H), 2.66 (s, 6H), 2.13 (s, 3H). MS (ES+): 246 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742132B2
Source datasetuspto-grants-2014_06
ORD IDord-22a34c66d1ce4dea8d79043b3af412ee
Source noteuspto-grants-2014_06