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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594905Generated: October 31, 2026

Potassium Phosphate, Tribasic → US8975415, RP53b

https://huagongshe.com/reaction/594905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Reactant5-(1-Propynyl)pyridine-3-boronic Acid (contains varying amounts of Anhydride)HCID 57416482—
Reactant6'-Bromodispiro[1,3-oxazole-4,4'-chromene-3',3''-oxetan]-2-amineHCID 86724312—
Catalyst(1E,4E)-1,5-diphenyl-1,4-pentadien-3-one palladiumHCID 15673654—
SolventDimethylformamideHCID 6228—
ProductUS8975415, RP53bHCID 8672431142.9%

Reaction Conditions

Temperature110 °C

Reaction Steps

The mixture of 6′-bromodispiro[1,3-oxazole-4,4′-chromene-3′,3″-oxetan]-2-amine (650 mg, 2.00 mmol), [5-(prop-1-yn-1-yl)pyridin-3-yl]boronic acid (644 mg, 4.00 mmol), (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one-palladium (3:2) (92 mg, 0.10 mmol), dicyclohexyl(2′,6′-dimethoxybiphenyl-2-yl)phosphine (164 mg, 0.400 mmol), and K3PO4 (1.70 g, 8.00 mmol) in DMF (13 mL) was stirred for 16 hours at 110° C. under argon atmosphere. The precipitate formed was removed by filtration with celite and washed with CHCl3. The filtrate was concentrated in vacuo. The residue was purified by silica gel chromatography (CHCl3:MeOH=99:1-95:5) to give 6′-[5-(prop-1-yn-1-yl)pyridin-3-yl]dispiro[1,3-oxazole-4,4′-chromene-3′,3″-oxetan]-2-amine (310 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242973B2
Source datasetuspto-grants-2016_01
ORD IDord-a8358e7f9fdd49e48cd37310ced664ad
Source noteuspto-grants-2016_01