HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509173Generated: November 2, 2026
HCID 86683589, compound → HCID 67253758, compound
https://huagongshe.com/reaction/1509173
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 86683589 | HCID 86683589 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 67253758 | HCID 67253758 | 62% |
Reaction Steps
tert-Butyl 1-(4-(1-cyclopentyl-2-oxo-7-phenyl-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazin-6-yl)phenyl)cyclobutylcarbamate (12 mg, 0.022 mmol) was dissolved in TFA (2 mL) and stirred for 30 seconds. The solution was immediately concentrated to dryness under reduced pressure. The residue was dissolved in diethyl ether (˜2 mL) and concentrated to dryness under reduced pressure three times. The residue was then slurried in diethyl ether (2 mL) and after settling the supernatant solvent removed by pipette. This was repeated three times. The remaining solvent was removed by freeze drying overnight to give the desired compound as an off-white solid (6 mg, 49% yield). 1H-NMR (500 MHz, MeOD) δ 7.60 (1H, s), 7.40 (2H, d), 7.36 (2H, d), 7.25-7.36 (3H, m), 7.18-7.25 (2H, m), 4.91 (1H, quin), 4.84 (2H, s), 2.66-2.31 (2H, m), 2.47-2.61 (2H, m), 2.12-2.31 (3H, m), 1.83-2.12 (5H, m), 1.63-1.81 (2H, m). LCMS (Method A) RT=4.55 min, M+2H+=441.19.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09221838B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-7cf1a5acd587425abd40bc3a806fc6d4 |
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| Source note | uspto-grants-2015_12 |
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