HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522961Generated: November 3, 2026
Trifluoroacetic acid → HCID 73295447, compound
https://huagongshe.com/reaction/522961
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 131735551 | HCID 131735551 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ammonium Hydroxide | HCID 14923 | — |
| Product | HCID 73295447 | HCID 73295447 | 51% |
Reaction Steps
To a solution of N-tert-butyl-2-(5-methylpyrazin-2-ylamino)-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide (72 mg, 158 mol) in dichloromethane (2.5 mL) was added trifluoroacetic acid (360 mg, 243 μL, 3.16 mmol) and stirred at room temperature for 16 h. The reaction mixture was concentrated in vacuo and the residue obtained diluted with dichloromethane (2.5 mL), methanol (1.2 mL) and ammonium hydroxide (0.35 mL) and the mixture 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-(5-methylpyrazin-2-ylamino)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide (26 mg, 79.9 mol, 51%) as a light green solid. 1H NMR (400 MHz, DMSO-d) δ ppm: 12.45 (s, 1H), 10.12 (s, 1H), 9.17 (d, J=1.5, 1 H), 8.40 (s, 1H), 8.21 (s, 1H), 8.10 (d, J=3.2, 1 H), 7.73 (s, 1H), 2.42 (s, 3H), 1.46 (s, 9H); MS (EI/CI) m/z: 326.1 [M+H].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09334278B2 |
|---|
| Source dataset | uspto-grants-2016_05 |
|---|
| ORD ID | ord-0cc25d262f204474a6c981f720fb6755 |
|---|
| Source note | uspto-grants-2016_05 |
|---|