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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277334Generated: October 26, 2026

Ammonia → 7-Cyclobutyl-3-phenyl-1,2,4-triazolo[4,3-b]pyridazin-6-ylamine

https://huagongshe.com/reaction/277334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant6-Chloro-7-cyclobutyl-3-phenyl-1,2,4-triazolo[4,3-b]pyridazineHCID 11000593—
SolventMethanolHCID 887—
Product7-Cyclobutyl-3-phenyl-1,2,4-triazolo[4,3-b]pyridazin-6-ylamineHCID 18314534—

Reaction Conditions

Temperature50 °C

Reaction Steps

6-Chloro-7-cyclobutyl-3-phenyl-1,2,4-triazolo[4,3-b]pyridazine (200 mg, 0.70 mmol) was suspended in methanol (8 ml). The mixture was saturated with ammonia and heated in a sealed tube at 50° C. overnight. The mixture was evaporated in vacuo, triturated (diethyl ether/hexane) and dried to give the title compound 1H NMR (360 MHz, d6-DMSO) δ 1.82-1.87 (1H, m), 1.99-2.35 (5H, m), 3.54-3.64 (1H, m), 7.34 (2H, vbs), 7.48-7.62 (3H, m), 8.08 (1H, s), 8.41 (2H, d, J=7.1 Hz); MS (ES+) m/e 266 [MH]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06355798B1
Source datasetuspto-grants-2002_03
ORD IDord-2476d77e89a2475abdc8ae6dd6696c6f
Source noteuspto-grants-2002_03