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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548917Generated: October 30, 2026

6-{[3-(5-Chloro-pyridin-2-yl)-5-methyl-isoxazol-4-ylmethyl]-amino}-pyridazine-3-carboxylic acid ethyl ester → 6-{[3-(5-Chloro-pyridin-2-yl)-5-methyl-isoxazol-4-ylmethyl]-amino}-pyridazine-3-carboxylic acid

https://huagongshe.com/reaction/548917

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-{[3-(5-Chloro-pyridin-2-yl)-5-methyl-isoxazol-4-ylmethyl]-amino}-pyridazine-3-carboxylic acid ethyl esterHCID 67157684—
Reactant5-[3-(4-Chloro-phenyl)-isoxazol-4-ylmethoxy]-pyrazine-2-carboxylic acid methyl esterHCID 67157839—
Product6-{[3-(5-Chloro-pyridin-2-yl)-5-methyl-isoxazol-4-ylmethyl]-amino}-pyridazine-3-carboxylic acidHCID 6715772492%

Reaction Steps

As described for example 112a, 6-{[3-(5-chloro-pyridin-2-yl)-5-methyl-isoxazol-4-ylmethyl]-amino}-pyridazine-3-carboxylic acid ethyl ester (405 mg, 1.1 mmol) was converted, instead of 5-[3-(4-chloro-phenyl)-isoxazol-4-ylmethoxy]-pyrazine-2-carboxylic acid methyl ester, to the title compound (346 mg, 92%) which was obtained as an off white solid. MS: m/e=343.9 [M−H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943619B2
Source datasetuspto-grants-2011_05
ORD IDord-17fe4f5097ed49fd8885cbaeb79cec08
Source noteuspto-grants-2011_05