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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271105Generated: October 31, 2026

4-Methoxyphenylhydrazine hydrochloride → HCID 178488389, compound

https://huagongshe.com/reaction/2271105

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxyphenylhydrazine hydrochlorideHCID 2723904—
ReactantHCID 18329922HCID 18329922—
Solvent1-ButanolHCID 263—
ProductHCID 178488389HCID 17848838921%

Reaction Steps

A mixture of ethyl 4-chloro-3-(4-methoxyphenyl)-2-methyl-5-pyridinecarboxylate (0.1842 g, 0.602 mmol) and 4-methoxyphenylhydrazine hydrochloride (0.1000 g, 0.724 mmol) in anhydrous 1-butanol (7 ml) was degassed by evaporating the flask under vacuum and refilling with nitrogen several times. The mixture was then stirred at reflux under nitrogen for 32 h, during which time more 4-methoxyphenylhydrazine hydrochloride (0.1001 g, 0.724 mmol) was added. The solvent was removed in vacuo and the residue was purified by flash chromatography (silica gel, 3-7% MeOH/CH2Cl2) to give 45.5 mg (21%) of the title compound as a yellow solid; mp 274-282° C. (CH2Cl2-MeOH-EtOAc); 1H NMR (360 MHz, DMSO-d6) δ2.40 (3H, s), 3.88 (3H, s), 3.96 (3H, s), 7.08 (2H, d, J 9.2 Hz), 7.19 (2H, d, J 8.7 Hz), 7.59 (2H, d, J 8.7 Hz), 8.11 (2H, d, J 9.1 Hz), 8.61 (1H, s), 12.43 (1H, br s); MS (ES+) m/z 362 MH]+. Anal. found: C, 69.95; H, 5.02; N, 11.60. C21H19N3O3 requires: C, 69.79; H, 5.30; N, 11.63%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06333336B1
Source datasetuspto-grants-2001_12
ORD IDord-1147efddcf5947c7a9ebd678f993741f
Source noteuspto-grants-2001_12