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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40212Generated: October 26, 2026

3-Hydrazinyl-6-phenylpyridazine → 3-Methoxy-6-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)quinoline

https://huagongshe.com/reaction/40212

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Hydrazinyl-6-phenylpyridazineHCID 6409842—
ReactantTert-butyl 2-(3-methoxyquinolin-6-yl)acetateHCID 59843087—
SolventHydrochloric AcidHCID 313—
Product3-Methoxy-6-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)quinolineHCID 57691355—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of tert-butyl 2-(3-methoxyquinolin-6-yl)acetate (148 mg) and 1-(6-phenylpyridazin-3-yl)hydrazine (126 mg) in HCl (conc., 0.3 mL) was heated at 100° C. for 5 min and was subject to microwave heating (180° C., 15 min) The yellow sludge was quenched with NaOH (5N, 1 mL). The pink mixture was filtered and washed with NaOH (1 N, 1 mL), H2O (2 mL). The solid was suspended in DMF (2 mL)-DCM (2 mL). MeI (0.2 mL) was added followed by the addition of NaOH (2N, 1 mL). After 2 h, the mixture was partitioned between DCM (10 mL) and aqueous Na2SO3 (5 mL). The organic was dried over MgSO4, concentrated, and purified in silica (1-15% MeOH in DCM) to give the product as a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524900B2
Source datasetuspto-grants-2013_09
ORD IDord-ac00229e44b74023bf42debc5b683c56
Source noteuspto-grants-2013_09