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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548843Generated: October 29, 2026

4-Aminotetrahydropyran → 4-Methyl-6-(5-methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridazine-3-carboxylic acid (tetrahydro-pyran-4-yl)-amide

https://huagongshe.com/reaction/548843

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminotetrahydropyranHCID 419223—
Reactant6-(5-Methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridazine-3-carboxylic acidHCID 66598975—
Reactant4-Methyl-6-(5-methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridazine-3-carboxylic acidHCID 67158153—
Product4-Methyl-6-(5-methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridazine-3-carboxylic acid (tetrahydro-pyran-4-yl)-amideHCID 4262965262%

Reaction Steps

As described for example 11b, 4-methyl-6-(5-methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridazine-3-carboxylic acid (200 mg, 0.61 mmol), instead of 6-(5-methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridazine-3-carboxylic acid, was converted, using 4-amino-tetrahydropyran instead of thiomorpholine 1,1-dioxide, to the title compound (SiO2, heptane:ethyl acetate=100:0 to 60:40, 156 mg, 62%) which was obtained as a white solid. MS: m/e=409.3 [M+H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943619B2
Source datasetuspto-grants-2011_05
ORD IDord-a53ae8f1fc20486fb438fd36e765d249
Source noteuspto-grants-2011_05