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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925442Generated: October 30, 2026

Potassium Phosphate, Tribasic → 5-[3-(6-Bromo-1-methyl-1H-indazol-3-ylamino)-phenyl]-5-methyl-morpholin-3-one

https://huagongshe.com/reaction/925442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Reactant6-Bromo-1-methyl-1H-indazol-3-amineHCID 46835549—
Reactant5-(3-Bromophenyl)-5-methylmorpholin-3-oneHCID 58155305—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
Product5-[3-(6-Bromo-1-methyl-1H-indazol-3-ylamino)-phenyl]-5-methyl-morpholin-3-oneHCID 89500193—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 5-(3-bromo-phenyl)-5-methyl-morpholin-3-one [Example 1, step f)] (CAS registry 1262858-67-2) (138.5 mg, 0.513 mmol), 6-bromo-1-methyl-1H-indazol-3-ylamine (CAS registry 1214899-85-0) (116 mg, 0.513 mmol), X-phos (78 mg, 0.164 mmol) and K3PO4 (218 mg, 1.025 mmol) in toluene (2.5 ml) and water (0.250 ml) was degassed with argon (5 min), then Pd2(dba)3 (37.6 mg, 0.041 mmol) was added and the reaction mixture was stirred at 120° C. for 20 h. The reaction mixture was diluted with water, sat. aq. NaHCO3 soln. and EtOAc. The layers were separated and the aq. layer was twice reextracted with EtOAc. The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated. The resulting crude product was purified by RP-HPLC (Waters SunFire C18 column, 5 μM, 19×150 mm, gradient 10 to 70% ACN+0.1% TFA) to yield the title compound as a pale yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284284B2
Source datasetuspto-grants-2016_03
ORD IDord-7dc8aa5297e74ee299e2b9d0d522908f
Source noteuspto-grants-2016_03