Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863934Generated: November 2, 2026

Hydrazine hydrate (1:1) → HCID 34176375, compound

https://huagongshe.com/reaction/1863934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant5-Chloro[1,2,4]triazolo[1,5-c]pyrimidineHCID 12603817—
SolventEthanolHCID 702—
ProductHCID 34176375HCID 34176375—

Reaction Steps

A solution of 155 mg (1 mmol) of 5-chloro[1,2,4]triazolo[1,5-c]pyrimidine [D. J. Brown and K. Shinozuka, Aust. J. Chem., 33, 1147 (1980)] in 6 mL of dry ethanol was added gradually to a vigorously stirred solution of 198 mg (204 mg, 4 mmol) of hydrazine monohydrate in 2 mL of dry ethanol. A white precipitate separated during the addition. After 1.5 h, the solid was collected on a filter. It was suspended in 2 mL of concentrated ammonium hydroxide and agitated for a few minutes. The solid was then collected on a filter and washed with some additional concentrated ammonium hydroxide, then with some ethanol, and finally with a large volume of diethyl ether. After drying, the title compound was obtained as a white solid, mp 245-246° C. (decomposition). LC-MS 151 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625888B2
Source datasetuspto-grants-2009_12
ORD IDord-7c66aa33cfc743a6a46ae284730bdea5
Source noteuspto-grants-2009_12