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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652162Generated: October 30, 2026

Methylhydrazine → HCID 178473786, compound

https://huagongshe.com/reaction/652162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylhydrazineHCID 6061—
ReactantHCID 14032496HCID 14032496—
Solvent1-ButanolHCID 263—
ProductHCID 178473786HCID 178473786—

Reaction Steps

A solution of 3.3 g of 4-(4-bromo-2-fluorobenzoyl)-1-acetylpiperidine, 1.1 g (0.013 mole) of methylhydrazine and 30 ml of n-butanol was heated under reflux for 16 hrs. The reaction mixture was concentrated in vacuo and the residue was diluted with water. The aqueous suspension was made basic with ammonium hydroxide solution and extracted with dichloromethane. The extract was washed with water, dried over anhydrous potassium carbonate and the solvent was concentrated to give 3-(1-acetyl-4-piperidinyl)-6-bromo-1H-indazole, as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04670447
Source datasetuspto-grants-1987_06
ORD IDord-55f71f21b5e54e3abfadf50f3f0f2729
Source noteuspto-grants-1987_06