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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509262Generated: October 30, 2026

2-Hydroxyacetohydrazide → HCID 86683643, compound

https://huagongshe.com/reaction/1509262

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-HydroxyacetohydrazideHCID 350536—
ReactantTert-butyl (1-(4-(7-phenyl-2-thioxo-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazin-6-yl)phenyl)cyclobutyl)carbamateHCID 86683631—
SolventP-XyleneHCID 7809—
ProductHCID 86683643HCID 8668364315%

Reaction Conditions

Temperature150 °C

Reaction Steps

A suspension of tert-butyl(1-(4-(7-phenyl-2-thioxo-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazin-6-yl)phenyl)cyclobutyl)carbamate (250 mg, 0.513 mmol) and 2-hydroxyacetohydrazide (230 mg, 2.56 mmol) in p-xylene (1.5 ml) was heated to 150° C. for 30 minutes under microwave irradiation. The resulting reaction mixture was concentrated to dryness under reduced pressure and purified by Biotage silica gel chromatography (gradient 0% to 20% ethyl acetate in n-hexanes) to give the title compound (40 mg, 15%). LCMS (Method D): RT=1.297 min, M+1=526. 1H NMR (500 MHz, CDCl3) δ 8.33 (1H, s), 7.37-7.32 (2H, m), 7.31-7.27 (5H, m), 7.25-7.20 (2H, m), 5.59 (2H, s), 5.06 (2H, bs), 5.02 (1H, bs), 2.53-2.43 (4H, m), 2.14-2.02 (1H, m), 1.88-1.76 (1H, m), 1.45-1.27 (9H, bs).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221838B2
Source datasetuspto-grants-2015_12
ORD IDord-dcc26d9210514791aa285c389063004a
Source noteuspto-grants-2015_12