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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509182Generated: October 30, 2026

HCID 86683594, compound → HCID 53262183, compound

https://huagongshe.com/reaction/1509182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86683594HCID 86683594—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 53262183HCID 5326218355.5%

Reaction Steps

Tert-butyl (1-(4-(1-methyl-8-phenyl-4H-pyrido[2,3-b][1,2,4]triazolo[4,3-d][1,4]oxazin-7-yl)phenyl)cyclobutyl)carbamate (11 mg, 0.022 mmol) was dissolved in TFA (1 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. This was repeated three times. The residue was then slurred in diethyl ether (2 ml) and after settling the supernatant solvent removed by pipette. This was repeated three times. The residue was then slurred in n-hexanes (2 ml) and after settling the supernatant solvent removed by pipette. This was repeated three times. The remaining solvent was removed under reduced pressure and the residue was dried to give the desired product as an off-white solid (5 mg, 55% yield). LCMS (Method A): RT=3.71 min, M+1=411. 1H-NMR (500 MHz, CD3OD) δ 8.11 (1H, s), 7.49-7.44 (2H, d), 7.42-7.37 (2H, d), 7.35-7.30 (3H, m), 7.29-7.25 (2H, m), 5.63 (2H, s), 2.84 (3H, s), 2.80-2.70 (2H, m), 2.61-2.51 (2H, m), 2.28-2.17 (1H, m), 2.01-1.88 (1H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221838B2
Source datasetuspto-grants-2015_12
ORD IDord-c60ec423afa4481d88e4df140ffd5dde
Source noteuspto-grants-2015_12