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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925465Generated: October 31, 2026

Binap, (A+-)- → 2-[6-((3R,6R)-5-{[Bis-(4-methoxy-phenyl)-phenyl-methyl]-amino}-3,6-dimethyl-6-trifluoromethyl-3,6-dihydro-2H-[1,4]oxazin-3-yl)-5-fluoro-pyridin-2-ylamino]-nicotinonitrile

https://huagongshe.com/reaction/925465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBinap, (A+-)-HCID 634876—
Reactant2-Amino-3-cyanopyridineHCID 818259—
ReactantSodium t-butoxideHCID 23676156—
Reactant[Bis-(4-methoxy-phenyl)-phenyl-methyl]-[(2R,5R)-5-(6-bromo-3-fluoro-pyridin-2-yl)-2,5-dimethyl-2-trifluoromethyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-amineHCID 89500352—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
Product2-[6-((3R,6R)-5-{[Bis-(4-methoxy-phenyl)-phenyl-methyl]-amino}-3,6-dimethyl-6-trifluoromethyl-3,6-dihydro-2H-[1,4]oxazin-3-yl)-5-fluoro-pyridin-2-ylamino]-nicotinonitrileHCID 90387331—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of [bis-(4-methoxy-phenyl)-phenyl-methyl]-[(2R,5R)-5-(6-bromo-3-fluoro-pyridin-2-yl)-2,5-dimethyl-2-trifluoromethyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-amine (250 mg, 0.372 mmol) in toluene (3.72 ml) was added 2-amino-3-pyridinecarbonitrile (221 mg, 1.859 mmol), Pd2(dba)3 (6.81 mg, 7.43 μmol), BINAP (9.26 mg, 0.015 mmol) and sodium tert-butoxide (50 mg, 0.520 mmol). The reaction mixture was degassed for 5 min and the microwave vial was sealed and stirred at 100° C. for 9 h. The reaction mixture was diluted with DCM and washed with water. The organic layer was dried with Na2SO4. The residue was purified by chromatography (silica gel; eluent DCM/MeOH+NH4OH) to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284284B2
Source datasetuspto-grants-2016_03
ORD IDord-df6dc3d85fc5496fb3e6c86391c95af7
Source noteuspto-grants-2016_03