HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522983Generated: October 29, 2026
Trifluoroacetic acid → HCID 73295613, compound
https://huagongshe.com/reaction/522983
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 131735559 | HCID 131735559 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ammonium Hydroxide | HCID 14923 | — |
| Product | HCID 73295613 | HCID 73295613 | 12% |
Reaction Steps
To a solution of N-tert-butyl-2-(2,4-dimethylphenylamino)-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide (82 mg, 175 mol) in dichloromethane (2.7 mL) was added trifluoroacetic acid (400 mg, 270 μL, 3.51 mmol) and the mixture stirred at room temperature for 16 h. The reaction mixture was concentrated in vacuo and the residue obtained diluted with dichloromethane (3 mL), methanol (1.5 mL) and ammonium hydroxide (0.4 mL) and stirred at room temperature for 1 h. The mixture was concentrated and triturated with water. The solid was collected by filtration and washed with water and ether to give N-tert-butyl-2-(2,4-dimethylphenylamino)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide (7 mg, 20.7 mol, 12%) as a yellow solid. 1H NMR (400 MHz, CDCl3-d) δ ppm: 9.19 (s, 1H), 8.12 (d, J=3.0, 1 H), 7.95 (s, 1H), 7.86 (s, 1H), 7.50 (d, J=7.8, 1 H), 7.15 (s, 1H), 7.08 (d, J=8.2, 1 H), 6.33 (s, 1H), 2.38 (s, 3H), 2.34 (s, 1H), 1.49 (s, 9H); MS (EI/CI) m/z: 338.2 [M+H].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09334278B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-e858ed8077c148d7b2b329975cb14b50 |
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| Source note | uspto-grants-2016_05 |
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