HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522981Generated: October 29, 2026
Trifluoroacetic acid → HCID 73058384, compound
https://huagongshe.com/reaction/522981
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 131735558 | HCID 131735558 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ammonium Hydroxide | HCID 14923 | — |
| Product | HCID 73058384 | HCID 73058384 | 78.4% |
Reaction Steps
To a solution of N-tert-butyl-2-(3-methylisothiazol-5-ylamino)-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide (32 mg, 69.5 mol) in dichloromethane (1.2 mL) was added trifluoroacetic acid (158 mg, 107 μL, 1.39 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 (1.2 mL), methanol (0.6 mL) and ammonium hydroxide (0.15 mL) and stirred at room temperature for 2 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-(3-methylisothiazol-5-ylamino)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide (18 mg, 54.5 mol, 78.4%) as a brown solid. 1H NMR (400 MHz, DMSO-d) δ ppm: 12.55 (s, 1H), 11.39 (s, 1H), 8.15 (d, J=3.2, 1 H), 8.11 (s, 1H), 7.37 (s, 1H), 6.70 (s, 1H), 2.33 (s, 3H), 1.55 (s, 9H); MS (EI/CI) m/z: 331.1 [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-a9cb60912a6f4b8ab30696fd902cffa2 |
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| Source note | uspto-grants-2016_05 |
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