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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505506Generated: November 4, 2026

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

https://huagongshe.com/reaction/505506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant2-(3-Bromo-5-chlorophenoxy)-3-chloro-6-fluorobenzaldehyde fluorobenzaldehydeHCID 86624470—
SolventDimethyl SulfoxideHCID 679—
Product4-(3-bromo-5-chlorophenoxy)-5-chloro-1H-indazoleHCID 56833642—

Reaction Steps

A suspension of 2-(3-bromo-5-chlorophenoxy)-3-chloro-6-fluorobenzaldehyde fluorobenzaldehyde (4.5 kg; 12.36 moles; 1.0 eq.) in DMSO (18 L) was degassed, after which hydrazine monohydrate (6.192 kg; 123.7 moles; 10.0 eqs.) was added over 20 minutes at room temperature. The reaction solution was degassed again, stirred at room temperature for 15 minutes, heated to 73° C., and then aged for 16 hours. After the mixture was cooled to room temperature, isopropanol (15 L) and then water (40 L) were added, and the resulting mixture cooled to room temperature, filtered under pressure, and washed with isopropanol:water (1:2; 10 L), water (12 L), and heptane (12 L). The title product as a solid was obtained after drying at 30° C.-35° C. under vacuum for four days.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781454B2
Source datasetuspto-grants-2010_08
ORD IDord-3e5c46afdb11497aa17d5232d9467c19
Source noteuspto-grants-2010_08