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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1529382Generated: November 4, 2026

Potassium Phosphate, Tribasic → HCID 67959693, compound

https://huagongshe.com/reaction/1529382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantDicyclohexyl(2',4',6'-tripropyl-[1,1'-biphenyl]-2-yl)phosphineHCID 21081571—
Reactant2-Bromo-6-cyclopropylpyrazineHCID 45788305—
ReactantHCID 67959644HCID 67959644—
CatalystPalladium, tris[mu-[(1,2-eta:4,5-eta)-(1E,4E)-1,5-diphenyl-1,4-pentadien-3-one]]di-, compd. with trichloromethane (1:1)HCID 11029508—
ProductHCID 67959693HCID 6795969343%

Reaction Conditions

Temperature130 °C

Reaction Steps

A glass microwave reaction vessel was charged with 5-(6-cyclopropylpyrazin-2-yl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-tosyl-1H-indole (172 mg, 0.33 mmol), 2-bromo-6-cyclopropylpyrazine (80 mg, 0.40 mmol, Combi-Phos Catalysis Inc.), Pd2(dba)3 CHCl3 adduct (10 mg, 10.0 μmol), 2-(dicyclohexylphosphino)-2′,4′,6′-tri-1-propyl-1,1′-biphenyl (X-Phos) (10 mg, 0.020 mmol) and K3PO4 (213 mg, 1.00 mmol). The tube was sealed. The tube was evacuated under vacuum and back-filled with N2 (3×). Dioxane (1.9 mL) and water (0.18 mL) were added. The reaction was stirred and heated in a Initiator microwave reactor (Personal Chemistry, Biotage AB, Inc., Upssala, Sweden) at 130° C. for 20 min. Water was added and the mixture was extracted with EtOAc (3×). The combined organic layers were dried over anhydrous Na2SO4, filtered and concentrated. The crude was purified by silica gel chromatography, eluting with a gradient of 0-50% EtOAc in hexanes, to provide 3,5-bis(6-cyclopropylpyrazin-2-yl)-1-tosyl-1H-indole (72 mg, 0.14 mmol, 43% yield) as a red oil. MS (ESI, pos. ion) m/z: 508.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090593B2
Source datasetuspto-grants-2015_07
ORD IDord-a644577f2a3341bf814fe26b494e2de0
Source noteuspto-grants-2015_07