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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1521621Generated: October 30, 2026

Acetohydrazide → 7-Bromo-1-methyl-4,5-dihydro-[1,2,4]triazolo[4,3-a]quinoline

https://huagongshe.com/reaction/1521621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetohydrazideHCID 14039—
Reactant6-Bromo-3,4-dihydroquinoline-2(1H)-thioneHCID 57370990—
Solvent1-ButanolHCID 263—
SolventWaterHCID 962—
Product7-Bromo-1-methyl-4,5-dihydro-[1,2,4]triazolo[4,3-a]quinolineHCID 70977894—

Reaction Conditions

Temperature140 °C

Reaction Steps

To a stirred solution of 6-bromo-3,4-dihydroquinoline-2(1H)-thione (74-4; 1.0 g, 0.004 mol) in n-butanol (20 mL) was added acetic hydrazide (1.19 g, 0.016 mol) at room temperature. Reaction mass was allowed to stir at 140° C. for 5 h. The reaction mixture was cooled to room temperature, diluted with water (50 mL) and extracted with ethyl acetate (3×25 mL). The combined organic layer was washed with saturated aqueous sodium chloride solution, dried over sodium sulphate and concentrated under vacuum to afford the crude compound. Crude compound was purified by silica gel column chromatography to obtain title compound. MS (M+2): 266.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073929B2
Source datasetuspto-grants-2015_07
ORD IDord-c9729ef9400e45d68eec503bb955bbb0
Source noteuspto-grants-2015_07