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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472417Generated: October 31, 2026

Potassium Phosphate, Tribasic → (S)-7-(2,5-difluorophenyl)-3-(2-fluoropyridin-4-yl)-2',6'-dihydrospiro[chromeno[2,3-b]pyridine-5,3'-[1,4]oxazin]-5'-amine

https://huagongshe.com/reaction/1472417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant(2,5-Difluorophenyl)boronic acidHCID 2734335—
Reactant2-Fluoropyridine-4-boronic acidHCID 2783396—
Reactant(S)-3-bromo-7-iodo-2',6'-dihydrospiro[chromeno[2,3-b]pyridine-5,3'-[1,4]oxazin]-5'-amineHCID 58465904—
CatalystBis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II)HCID 11714597—
CatalystHCID 178418807HCID 178418807—
SolventWaterHCID 962—
Solvent2-MethyltetrahydrofuranHCID 7301—
Solvent1,4-DioxaneHCID 31275—
Product(S)-7-(2,5-difluorophenyl)-3-(2-fluoropyridin-4-yl)-2',6'-dihydrospiro[chromeno[2,3-b]pyridine-5,3'-[1,4]oxazin]-5'-amineHCID 5846592327.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

A vial was charged with 2,5-difluorophenylboronic acid (0.035 g, 0.222 mmol), PdCl2(dppf)-CH2Cl2 adduct (8.65 mg, 10.59 μmol), (S)-3-bromo-7-iodo-2′,6′-dihydrospiro[chromeno[2,3-b]pyridine-5,3′-[1,4]oxazin]-5′-amine (0.100 g, 0.212 mmol), and potassium phosphate (0.450 g, 2.118 mmol). Dioxane (2 mL) and water (1 mL) were added, the vial was flushed with argon, sealed and heated to 80° C. 1 hour. The reaction mixture was cooled to rt and bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II) (7.50 mg, 10.59 μmol) was added, followed by 2-fluoropyridin-4-ylboronic acid (0.045 g, 0.318 mmol). The reaction mixture was again capped under argon and was heated to 80° C. for and additional hour. The reaction mixture was then diluted with 2-MeTHF, dried over MgSO4 and concentrated. Purification of the crude residue by column chromatography [0-100% (95:5 EtOAc/MeOH)/DCM] gave (S)-7-(2,5-difluorophenyl)-3-(2-fluoropyridin-4-yl)-2′,6′-dihydrospiro[chromeno[2,3-b]pyridine-5,3′-[1,4]oxazin]-5′-amine (0.028 g, 0.059 mmol, 27.9% yield) as a light yellow solid. [M+H]+=475.0

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012446B2
Source datasetuspto-grants-2015_04
ORD IDord-4dd332c4ebfa459594111528a39b5675
Source noteuspto-grants-2015_04