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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097948Generated: October 29, 2026

Potassium Carbonate → 5-Bromo-1-(3-methoxy-phenyl)-1H-indazole

https://huagongshe.com/reaction/1097948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactanttrans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
Reactant2,5-DibromobenzaldehydeHCID 13540069—
Catalysttrans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
Product5-Bromo-1-(3-methoxy-phenyl)-1H-indazoleHCID 57421349—

Reaction Conditions

Temperature160 °C

Reaction Steps

3-Methoxyphenylhydrazine hydrochloride (1 g) was suspended in 1 M aqueous NaOH solution and extracted with ether. The organic phase was dried (MgSO4), filtered and concentrated to dryness to give 3-methoxyphenylhydrazine. 2,5-Dibromobenzaldehyde (1 g) and N-methylpyrrolidone (3.7 ml) were added and the mixture was heated under microwave conditions to 160° C. for 10 min. K2CO3 (1.015 g), Cul (36 mg) and trans-N,N′-dimethyl-cyclohexane-1,2-diamine (53 mg) were added and the mixture was heated under microwave conditions to 160° C. for 40 min. Cul (18 mg) and trans-N,N′-dimethyl-cyclohexane-1,2-diamine (26 mg) were added and the mixture was heated under microwave conditions to 160° C. for 20 min. The mixture was filtered and the filtrate was concentrated. The product was purified by chromatography (SiO2, CH2Cl2/MeOH 100:0=>95:5) to give the title compound (659 mg) as a yellow oil. MS (m/e)=303.0 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143280B2
Source datasetuspto-grants-2012_03
ORD IDord-c2acd165de544841a5f06fbea009df5f
Source noteuspto-grants-2012_03