Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174286Generated: October 29, 2026

Ammonium Hydroxide → HCID 69093139, compound

https://huagongshe.com/reaction/2174286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 69093586HCID 69093586—
CatalystHCID 178419072HCID 178419072—
SolventEthylene glycol dioxaneHCID 22419261—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 69093139HCID 6909313959.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirring suspension of 4-(3-(4-bromopyridin-2-yl)-1-(2-fluorobenzyl)-1H-1,2,4-triazol-5-yl)thiazole (I-51, 1 eq) and copper(I) oxide (1 eq) in ethylene glycol-dioxane (approx. 4:1) in a sealed tube was added ammonium hydroxide. The resultant reaction mixture was heated at 100° C. for 12 h and then cooled to room temperature, treated with brine and extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate, concentrated and purified using SiO2 chromatography (methylene chloride/acetonitrile/methanol) to afford 2-(1-(2-fluorobenzyl)-5-(thiazol-4-yl)-1H-1,2,4-triazol-3-yl)pyridin-4-amine as a solid in 59.6% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09061030B2
Source datasetuspto-grants-2015_06
ORD IDord-c13fa0fed2db4d09ab4b136ac390eb16
Source noteuspto-grants-2015_06