Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509173Generated: November 2, 2026

HCID 86683589, compound → HCID 67253758, compound

https://huagongshe.com/reaction/1509173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86683589HCID 86683589—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 67253758HCID 6725375862%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221838B2
Source datasetuspto-grants-2015_12
ORD IDord-7cf1a5acd587425abd40bc3a806fc6d4
Source noteuspto-grants-2015_12