Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111122Generated: October 26, 2026

O-(2-(Vinyloxy)ethyl)hydroxylamine → 4-(2-fluoro-4-(methylthio)phenylamino)-N-(2-hydroxyethoxy)-1,5-dimethyl-6-oxo-1,6-dihydropyridazine-3-carboxamide

https://huagongshe.com/reaction/2111122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-(2-(Vinyloxy)ethyl)hydroxylamineHCID 21867017—
ReactantEthyl 4-(2-fluoro-4-(methylthio)phenylamino)-1,5-dimethyl-6-oxo-1,6-dihydropyridazine-3-carboxylateHCID 66674013—
Product4-(2-fluoro-4-(methylthio)phenylamino)-N-(2-hydroxyethoxy)-1,5-dimethyl-6-oxo-1,6-dihydropyridazine-3-carboxamideHCID 1666715878%

Reaction Steps

The title compound was prepared in 78% yield (2 steps) by the procedures described in Example 166 (steps I and J) using ethyl 4-(2-fluoro-4-(methylthio)phenylamino)-1,5-dimethyl-6-oxo-1,6-dihydropyridazine-3-carboxylate (50 mg, 0.14 mmol) and O-(2-vinyloxy-ethyl)-hydroxylamine (44 mg, 0.43 mmol). MS APCI (−) m/z 381 (M−1) detected; 1H NMR (400 MHz, CD3OD) δ 7.10 (dd, 1H), 7.03 (dd, 1H), 6.87 (t, 1H), 3.99 (t, 2H), 3.79 (s, 3H), 3.74 (t, 2H), 2.47 (s, 3H), 1.74 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517994B2
Source datasetuspto-grants-2009_04
ORD IDord-0715319cfd544af392bb34f6ccf9742c
Source noteuspto-grants-2009_04