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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509207Generated: November 1, 2026

HCID 67256553, compound → HCID 53262410, compound

https://huagongshe.com/reaction/1509207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67256553HCID 67256553—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 53262410HCID 5326241060.8%

Reaction Steps

tert-Butyl 1-(4-(2-oxo-7-phenyl-1-(pyridin-3-yl)-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazin-6-yl)phenyl)cyclobutylcarbamate (30 mg, 0.055 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 (15 mg, 49% yield). 1H-NMR (500 MHz, MeOD) δ 8.62-8.77 (2H, m), 7.98 (1H, d), 7.68 (1H, dd), 7.36 (2H, d), 7.39 (2H, d), 7.15-7.24 (3H, m), 6.97-7.05 (2H, m), 6.77 (1H, s), 5.14 (2H, s), 2.66-2.77 (2H, m), 2.46-2.58 (2H, m), 2.13-2.25 (1H, m), 1.86-1.97 (1H, m). LCMS (Method A) RT=3.71 min, M+2H+=450.20.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221838B2
Source datasetuspto-grants-2015_12
ORD IDord-7499e1189cd34326bb6155f13b143c44
Source noteuspto-grants-2015_12