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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046590Generated: November 1, 2026

Pyridazine-4-carboxylic Acid → Pyridazine-4-carboxylic acid(1-{(rac) 3-[5-chloro-3-fluoro-2-(5-methyl-[1,2,4]oxadiazol-3-yl)-phenyl]-6,7-dihydro-5H-[1]pyrindin-7-ylcarbamoyl}-cyclopropyl)-amide

https://huagongshe.com/reaction/2046590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridazine-4-carboxylic AcidHCID 2761046—
Reactant1-Amino-cyclopropanecarboxylic acid {(rac)-3-[5-chloro-3-fluoro-2-(5-methyl-[1,2,4]oxadiazol-3-yl)-phenyl]-6,7-dihydro-5H-[1]pyrindin-7-yl}-amideHCID 60142961—
ProductPyridazine-4-carboxylic acid(1-{(rac) 3-[5-chloro-3-fluoro-2-(5-methyl-[1,2,4]oxadiazol-3-yl)-phenyl]-6,7-dihydro-5H-[1]pyrindin-7-ylcarbamoyl}-cyclopropyl)-amideHCID 60142963—

Reaction Steps

In analogy to the procedure described for the preparation of intermediate A-1 [B], 1-amino-cyclopropanecarboxylic acid{(rac)-3-[5-chloro-3-fluoro-2-(5-methyl-[1,2,4]oxadiazol-3-yl)-phenyl]-6,7-dihydro-5H-[1]pyrindin-7-yl}-amide (example 37) has been coupled with pyridazine-4-carboxylic acid to yield the title compound as light brown amorphous solid. MS: 534.1 (MH+, 1Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592426B2
Source datasetuspto-grants-2013_11
ORD IDord-2abb87f02ef3400198091a658f66203f
Source noteuspto-grants-2013_11