HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522965Generated: October 30, 2026
Trifluoroacetic acid → HCID 73295445, compound
https://huagongshe.com/reaction/522965
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 131735553 | HCID 131735553 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ammonium Hydroxide | HCID 14923 | — |
| Product | HCID 73295445 | HCID 73295445 | 77.4% |
Reaction Steps
To a solution of N-tert-butyl-2-(pyridin-3-ylamino)-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide (44 mg, 99.9 mol) in dichloromethane (1.6 mL) was added trifluoroacetic acid (228 mg, 154 μL, 2.00 mmol) and the reaction mixture stirred at room temperature for 16 h. The reaction mixture was concentrated in vacuo and the residue obtained diluted with dichloromethane (1.6 mL), methanol (0.8 mL) and ammonium hydroxide (0.2 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-(pyridin-3-ylamino)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide (24 mg, 77.3 mol, 77%) as a brown solid. 1H NMR (400 MHz, DMSO-d) δ ppm: 12.26 (s, 1H), 9.54 (s, 1H), 8.77 (d, J=2.5, 1 H), 8.04 (d, J=4.6, 1 H), 7.98 (d, J=8.5, 1 H), 7.92 (d, J=3.3, 1 H), 7.91 (s, 1H), 7.57 (s, 1H), 7.19 (m, 1H), 1.31 (s, 9H); MS (EI/CI) m/z: 311.1 [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-0b7c41de0d3f480882505cf10beb6ca5 |
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| Source note | uspto-grants-2016_05 |
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