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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570910Generated: October 30, 2026

Pyridine → HCID 89601899, compound

https://huagongshe.com/reaction/570910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
ReactantHCID 89601756HCID 89601756—
SolventMethanolHCID 887—
ProductHCID 89601899HCID 89601899—

Reaction Steps

To a solution of tert-butyl 4-[acetyl(tert-butoxycarbonyl)amino]-6-formyl-3-oxo-5H-1,2,4-triazine-2-carboxylate (1.15 g, 3.00 mmol) in MeOH (1.8 mL) at room temperature was added pyridine (0.88 mL, 10.9 mmol) followed by O-methylhydroxylamine HCl salt (376 mg, 4.50 mmol). The obtained mixture was stirred for 20 h at room temperature and then concentrated under reduced pressure. The residual was redissolved in EtOAc, washed with water and dried (Na2SO4). After evaporation of the solvent, the crude product was obtained as a viscous oil which was used in the subsequent step without further purification. LCMS (Method I) RT 1.77 min. [M+H]+ 372.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09024019B2
Source datasetuspto-grants-2015_05
ORD IDord-b5e991b3b1e74e3ba89573da768cec54
Source noteuspto-grants-2015_05