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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505503Generated: October 27, 2026

Hydrazine hydrate (1:1) → 4-(3-bromo-5-chlorophenoxy)-5-chloro-1H-indazole

https://huagongshe.com/reaction/505503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant2-(3-Bromo-5-chlorophenoxy)-3-chloro-6-fluorobenzaldehydeHCID 56833553—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-(3-bromo-5-chlorophenoxy)-5-chloro-1H-indazoleHCID 56833642—

Reaction Steps

To a suspension of 2-(3-bromo-5-chlorophenoxy)-3-chloro-6-fluorobenzaldehyde (77.5 g, 213 mmol) in ethanol (120 mL) was added hydrazine hydrate (31 mL, 639 mmol). The resulting mixture was then heated at reflux for 4 days, after which the mixture was cooled to room temperature, diluted with water (100 mL) and the resulting solid was filtered. The solid was absorbed onto silica gel (300 g) and purified on a silica gel (1500 g) column (0-40% EtOAc/CH2Cl2) to give the title product as a white solid. LRMS (M+1)=358.8

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781454B2
Source datasetuspto-grants-2010_08
ORD IDord-2e3984c1570c4926a5f81b4cf3bf093c
Source noteuspto-grants-2010_08