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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574219Generated: October 27, 2026

Sodium Carbonate → (S)-2-(5-(3-Amino-6-methoxy-5-(trifluoromethyl)-4-vinylpyridin-2-yl)-1,3,4-oxadiazol-2-yl)-1,1,1-trifluoropropan-2-ol

https://huagongshe.com/reaction/574219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 5233012—
Reactant(S)-2-(5-(3-amino-4-chloro-6-methoxy-5-(trifluoromethyl)pyridin-2-yl)-1,3,4-oxadiazol-2-yl)-1,1,1-trifluoropropan-2-olHCID 71515814—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
Product(S)-2-(5-(3-Amino-6-methoxy-5-(trifluoromethyl)-4-vinylpyridin-2-yl)-1,3,4-oxadiazol-2-yl)-1,1,1-trifluoropropan-2-olHCID 86729605—

Reaction Conditions

Temperature130 °C

Reaction Steps

To a solution of (S)-2-(5-(3-amino-4-chloro-6-methoxy-5-(trifluoromethyl)pyridin-2-yl)-1,3,4-oxadiazol-2-yl)-1,1,1-trifluoropropan-2-ol (Ex 13.1) (160 mg, 0.393 mmol) in MeCN (1 ml) was added bis(triphenyl phosphine)palladium(II) chloride (Aldrich) (83 mg, 0.118 mmol) followed by 4,4,5,5-tetramethyl-2-vinyl-1,3,2-dioxaborolane (Sigma Aldrich)(0.087 ml, 0.511 mmol). 2M Sodium carbonate (0.885 ml, 1.770 mmol) was added and the resulting mixture was heated at 130° C. for 30 minutes using microwave radiation. The mixture was filtered through Celite® and washed through with EtOAc. The filtrate was diluted further with EtOAc (50 ml) and washed with sat.NaHCO3, water, brine and dried over MgSO4. Isolute Si-TMT (2,4,6-trimercaptotriazine silica, palladium scavenger) was added the mixture was stirred for 30 mins and filtered. The solvent was removed in vacuo to afford the title compound which was used without further purification;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034879B2
Source datasetuspto-grants-2015_05
ORD IDord-ff0c4be5d1e7443697c2f2c24ced8255
Source noteuspto-grants-2015_05