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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509234Generated: November 2, 2026

HCID 86683625, compound → HCID 53262458, compound

https://huagongshe.com/reaction/1509234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86683625HCID 86683625—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 53262458HCID 5326245848.4%

Reaction Steps

tert-Butyl 1-(4-(7-phenyl-1-(pyridin-3-yl)-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazin-6-yl)phenyl)cyclobutylcarbamate (10 mg, 0.019 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 (4 mg, 32% yield). 1H-NMR (500 MHz, MeOD) δ 8.57 (1H, br s), 8.28 (1H, br s), 7.80 (1H, d), 7.43 (1H, br s), 7.26 (2H, d), 7.24 (2H, d), 7.04-7.16 (4H, m), 6.90-7.00 (2H, m), 4.51 (2H, t), 3.80 (2H, t), 2.56-2.70 (2H, m), 2.37-2.52 (2H, m), 2.02-2.16 (1H, m), 1.74-1.90 (1H, m). LCMS (Method D) RT=0.77 min, M+H+=435.20.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221838B2
Source datasetuspto-grants-2015_12
ORD IDord-019df738946a4d9ab82c16d83dff7388
Source noteuspto-grants-2015_12