Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640203Generated: October 31, 2026

HCID 66721428, compound → HCID 58902470, compound

https://huagongshe.com/reaction/1640203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66721428HCID 66721428—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 58902470HCID 5890247094.9%

Reaction Steps

A solution of N-(3-tert-butylphenyl)-7-({2-[(4-methoxybenzyl)(methyl)amino]-pyridin-4-yl}oxy)-1,2,3,4-tetrahydronaphthalene-2-carboxamide (454 mg, 0.83 mmol) in DCM (4 mL) and TFA (4 mL) was heated at 50° C. for 18 h. The reaction mixture was allowed to cool to rt and the solvents were evaporated. The residue was purified by column chromatography to give N-(3-tert-butylphenyl)-7-{[2-(methylamino)pyridin-4-yl]oxy}-1,2,3,4-tetrahydronaphthalene-2-carboxamide (337 mg, 94.9%). LCMS: (FA) ES+ 430.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110687B2
Source datasetuspto-grants-2012_02
ORD IDord-488cb75d1cd44a67a9c069accd5e44ff
Source noteuspto-grants-2012_02