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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297484Generated: October 29, 2026

Hydroxyamine hydrochloride → N-hydroxy-4-(6-methoxy-4-thiazol-2-yl-phthalazin-1-yl)-butyramide

https://huagongshe.com/reaction/2297484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodiumHCID 5360545—
Reactant4-(6-Methoxy-4-thiazol-2-yl-phthalazin-1-yl)-butyric acid methyl esterHCID 54370004—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
ProductN-hydroxy-4-(6-methoxy-4-thiazol-2-yl-phthalazin-1-yl)-butyramideHCID 1838167928.6%

Reaction Steps

A solution of sodium (388 mg, 16.9 mmoles) in CH3OH (6 ml) was added with hydroxylamine hydrochloride (1.3 g, 18.71 mmoles). The resultant solution was added to a solution of 4-(6-methoxy-4-thiazol-2-yl-phthalazin-1-yl)-butyric acid methyl ester (1.5 g, 4.4 mmoles), prepared as described in example 115, in CH3OH (30 ml), and stirred at room temperature for 2 days, then refluxed for 7 hours. NH2OH.HCl (1.6 g) and sodium (450 mg) were added, and the mixture was refluxed. After 1 night further NH2OH.HCl (0.9 g) and sodium (257 mg) were added, and the mixture was refluxed for 24 hours. The precipitate was filtered off and the mother liquors dried, taken up in water and filtered. The resultant solid was chromatographed (eluent: CH2Cl2/CH3OH 95:5) to give a solid which was suspended in water, dissolved in 10% NaOH and precipitated with saturated ammonium chloride to give 430 mg of the title compound (yield: 28.6%). m.p.: 189-190° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492360B1
Source datasetuspto-grants-2002_12
ORD IDord-109c5c769c604d11b4fec2ebc6498fd2
Source noteuspto-grants-2002_12