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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509171Generated: November 2, 2026

HCID 86683588, compound → HCID 53262179, compound

https://huagongshe.com/reaction/1509171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86683588HCID 86683588—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 53262179HCID 53262179120.9%

Reaction Steps

tert-Butyl 1-(4-(1-isopropyl-2-oxo-7-phenyl-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazin-6-yl)phenyl)cyclobutylcarbamate (7 mg, 0.014 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 (7 mg, 97% yield). 1H-NMR (500 MHz, MeOD) δ 7.64 (1H, s), 7.41 (2H, d), 7.36 (2H, d), 7.26-7.32 (3H, m), 7.19-7.26 (2H, m), 4.80 (2H, s), 4.75 (1H, sep), 2.68-2.80 (2H, m), 2.50-2.62 (2H, m), 2.13-2.29 (1H, m), 1.89-2.00 (1H, m), 1.48 (6H, d). LCMS (Method A) RT=4.20 min, M+2H+=415.19.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221838B2
Source datasetuspto-grants-2015_12
ORD IDord-128bda28f8384d01856d9586ead6cf2f
Source noteuspto-grants-2015_12