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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803241Generated: November 1, 2026

Hydrazine → 5-(5-chloro-1-(4-(trifluoromethoxy)phenyl)pentyl)-N-(4-(4-chloro-1H-imidazol-1-yl)-3-methoxyphenyl)-1H-1,2,4-triazol-3-amine

https://huagongshe.com/reaction/1803241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
Reactant6-Chloro-2-(4-(trifluoromethoxy)phenyl)hexanoic acidHCID 58110183—
Reactantmethyl 4-(4-chloro-1H-imidazol-1-yl)-3-methoxyphenylcarbamimidothioate, hydroiodideHCID 178493236—
Product5-(5-chloro-1-(4-(trifluoromethoxy)phenyl)pentyl)-N-(4-(4-chloro-1H-imidazol-1-yl)-3-methoxyphenyl)-1H-1,2,4-triazol-3-amineHCID 668592919%

Reaction Steps

Methyl 4-(4-chloro-1H-imidazol-1-yl)-3-methoxyphenylcarbamimidothioate, hydroiodide (500 mg, 1.69 mmol, from preparation B) and 6-chloro-2-(4-(trifluoromethoxy)phenyl)hexanoic acid (523 mg, 1.685 mmol, from preparation AI) were coupled and then reacted with hydrazine (0.211 mL, 6.74 mmol) using a procedure analogous to Step A of Example 13. The crude products were purified using silica gel chromatography (40-100% ethyl acetate/chloroform) to afford 5-(5-chloro-1-(4-(trifluoromethoxy)phenyl)pentyl)-N-(4-(4-chloro-1H-imidazol-1-yl)-3-methoxyphenyl)-1H-1,2,4-triazol-3-amine (80 mg, 0.14 mmol, 9.0% yield) as a yellow residue. LC-MS (M+H)+ 555.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349880B2
Source datasetuspto-grants-2013_01
ORD IDord-38d9fda53ad14c9cb71c33eace427939
Source noteuspto-grants-2013_01