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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105533Generated: October 31, 2026

Hydroxylamine → HCID 11391154, compound

https://huagongshe.com/reaction/2105533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxylamineHCID 787—
ReactantHCID 69002385HCID 69002385—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11391154HCID 11391154—

Reaction Conditions

Temperature60 °C

Reaction Steps

The crude 2-(2,2-dimethyl-5-oxo-[1,3]dioxolan-4-yl)-4H-benzo[1,4]thiazin-3-one (0.036 mmol) is dissolved in 0.5 mL of THF and 0.5 mL of NH2OH (1N in MeOH) is added to the mixture. After the addition, the mixture is stirred at 60° C. for 3 hours. The solvent is then removed under vacuum and the residue is purified by preparative thin layer chromatography (silica gel, 10% MeOH/CH2Cl2) to provide the title compound 2,N-dihydroxy-2-(3-oxo-3,4-dihydro-2H-benzo[1,4]thiazin-2-yl)-acetamide. Yield: 70%. 1H NMR (400 MHz, MeOD) δ 7.30 (dd, 1H, J=1.29 Hz, J=8.0 Hz), 7.18, (dt, 1H, J=1.3 Hz, J=8.0 Hz), 7.01 (dt, 1H, J=1.3 Hz, J=8.0 Hz), 6.95 (dd, 1H, J=1.3 Hz, J=8.0 Hz), 4.74 (d, 1H, J=3.80), 3.97 (d, 1H, J=3.8). MS: (ES+): 255.1[M+1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579363B2
Source datasetuspto-grants-2009_08
ORD IDord-fb79e383032b4b478b188689b4a0aee2
Source noteuspto-grants-2009_08