HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522997Generated: October 29, 2026
Trifluoroacetic acid → HCID 73296111, compound
https://huagongshe.com/reaction/522997
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 90040937 | HCID 90040937 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 73296111 | HCID 73296111 | 92% |
Reaction Steps
N-(1-Hydroxy-2-methylpropan-2-yl)-2-(pyridin-3-ylamino)-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide (32 mg, 70.1 μmol) was dissolved in dichloromethane (1.2 mL) and treated with trifluoroacetic acid (160 mg, 108 μL, 1.4 mmol). The mixture was stirred at room temperature for 16 h. The mixture was concentrated then re-dissolved in dichloromethane (1 mL), methanol (0.5 mL) and ammonium hydroxide (0.2 mL) and the mixture stirred at room temperature for 1 h. The mixture was concentrated in vacuo then triturated with water and filtered. The solid obtained was washed with ether then dried to give N-(1-hydroxy-2-methylpropan-2-yl)-2-(pyridin-3-ylamino)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide (21 mg, 64.3 μmol, 92%) as a light yellow solid. 1H NMR (400 MHz, DMSO-d) 6 ppm: 12.39 (s, 1H), 9.66 (s, 1H), 8.85 (d, J=2.5, 1 H), 8.21 (m, 1H), 8.16 (dd, J=4.7, 1.6, 1 H), 8.04 (s, 1H), 8.03 (s, 1H), 7.67 (s, 1H), 7.33 (m, 1H), 5.05 (t, J=5.6, 1 H), 3.58 (d, J=5.9, 2 H), 1.36 (s, 6H); MS (EI/CI) m/z: 327.1 [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-8e4848251d2141fdb0e2f6864dc160da |
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| Source note | uspto-grants-2016_05 |
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