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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Bis-(1H-imidazol-2-YL)-methanone | HCID 5250894 | — |
| Reactant | (6-Dimethylaminomethyl-2-methyl-indolizin-3-yl)-acetic acid tert-butyl ester | HCID 68712027 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(6-Dimethylaminomethyl-2-methyl-indolizin-3-yl)-acetamide | HCID 59192021 | 91.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08742132B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-22a34c66d1ce4dea8d79043b3af412ee |
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| Source note | uspto-grants-2014_06 |
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