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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472085Generated: October 30, 2026

Hydrochloric Acid → N3-{2-methoxy-4-[4-(4-methyl-4-oxido-1,4-azaphosphinan-1-yl)piperidin-1-yl]-phenyl}-N5-[2-(propan-2-ylsulfonyl)phenyl]pyridazine-3,5-diamine

https://huagongshe.com/reaction/1472085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Methoxy-4-[4-(4-methyl-4-oxido-1,4-azaphosphinan-1-yl)piperidin-1-yl]anilineHCID 67053290—
Reactant6-chloro-N-[2-(propan-2-ylsulfonyl)phenyl]pyridazin-4-amineHCID 86668808—
SolventEthanolHCID 702—
Solvent2-MethoxyethanolHCID 8019—
ProductN3-{2-methoxy-4-[4-(4-methyl-4-oxido-1,4-azaphosphinan-1-yl)piperidin-1-yl]-phenyl}-N5-[2-(propan-2-ylsulfonyl)phenyl]pyridazine-3,5-diamineHCID 68165251—

Reaction Steps

To a solution of 6-chloro-N-[2-(propan-2-ylsulfonyl)phenyl]pyridazin-4-amine (prepared in Example 73: 0.02 mmol) and 2-methoxy-4-[4-(4-methyl-4-oxido-1,4-azaphosphinan-1-yl)piperidin-1-yl]aniline (0.7 mmol) in 1 mL of 2-Methoxy ethanol, is added 1 mL of 2.5M HCl in Ethanol. The reaction mixture is heated in a sealed tube at 140 degree until formation of the desired compound. The reaction mixture is filtered through a syringe filter and can be purified by Prep-HPLC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012462B2
Source datasetuspto-grants-2015_04
ORD IDord-81eeb2ba4538402daf6c279a5e375b48
Source noteuspto-grants-2015_04