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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904371Generated: November 2, 2026

Acetohydrazide → 6-[3,5-Dimethyl-1,2,4-triazol-4-yl]-2-methoxy-8-methylquinoline

https://huagongshe.com/reaction/1904371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetohydrazideHCID 14039—
ReactantPhosphorus pentachlorideHCID 24819—
Reactant6-Acetamido-2-methoxy-8-methylquinolineHCID 19867076—
SolventTolueneHCID 1140—
Product6-[3,5-Dimethyl-1,2,4-triazol-4-yl]-2-methoxy-8-methylquinolineHCID 1986708626.3%

Reaction Steps

Phosphorous pentachloride (1.0 g) was added to a stirred solution of 6-acetamido-2-methoxy-8-methylquinoline (1.0 g) in toluene (50 cm3) and the mixture was stirred at 50° for 15 minutes. Acetyl hydrazine (1.35 g) was then added and the mixture was stirred for 3 hours at 60°. The toluene was removed in vacuo, the residue dissolved in ethanol, and aqueous ammonia solution (S.G. 0.88) (25 cm3) was added. Dichloromethane (100 cm3) was added and the organic phase was separated. The aqueous phase was further extracted with dichloromethane (2×25 cm3), and the combined organic phases were dried (MgS04) and evaporated to give a solid which was chromatographed on silica (Merck "MK 60.9385" [Trade Mark]) eluting with dichloromethane:methanol, 19:1. Combination and evaporation of appropriate fractions afforded 6-[3,5-dimethyl-1,2,4-triazol-4-yl]-2-methoxy-8-methylquinoline (0.306 g), which was recrystallised from toluene to give microcrystals, m.p. 211°-213° (0.066 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04837334
Source datasetuspto-grants-1989_06
ORD IDord-13a0e1b13a44453e9fdb52d3cf660113
Source noteuspto-grants-1989_06