Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634229Generated: October 31, 2026

Potassium Phosphate, Tribasic → HCID 68328525, compound

https://huagongshe.com/reaction/634229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
ReactantHCID 49758247HCID 49758247—
ReactantHCID 68328226HCID 68328226—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 68328525HCID 6832852524.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a 5 mL glass microwave tube containing N-tert-butyl-5-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-tosyl-1H-indol-5-yl)-1,3,4-oxadiazol-2-amine (357.8 mg, 0.667 mmol) was added 2-bromo-4-cyclopropylpyrimidine (153 mg, 0.767 mmol) (CombiPhos Catalysts Inc.), potassium phosphate (425 mg, 2.001 mmol) (Sigma-Aldrich), dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (19.08 mg, 0.040 mmol) (Strem), and Pd2(dba)3 (18.32 mg, 0.020 mmol) (Strem). The tube was purged with argon, the solids were treated with Dioxane (3.0 mL) and Water (0.300 mL), the tube was sealed, and the contents were heated in an Initiator microwave reactor (Personal Chemistry, Biotage AB, Inc., Upssala, Sweden) at 120° C. for 20 min. The mixture was treated with H2O and extracted with EtOAc. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated. The crude material was purified by flash chromatography (eluting with 5-60% EtOAc in Hex) affording N-tert-butyl-5-(3-(4-cyclopropylpyrimidin-2-yl)-1-tosyl-1H-indol-5-yl)-1,3,4-oxadiazol-2-amine (86.2 mg, 0.163 mmol, 24.45) as an off-white foam. MS (ESI, pos. ion) m/z: 529.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321756B2
Source datasetuspto-grants-2016_04
ORD IDord-b92f148117d941d69f6cfcc963375e3f
Source noteuspto-grants-2016_04