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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912277Generated: October 31, 2026

Potassium Phosphate, Tribasic → HCID 59244850, compound

https://huagongshe.com/reaction/912277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
ReactantBis-(4-methoxybenzyl)-[5-(2-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-pyrimidin-2-yl]-amineHCID 45258862—
ReactantHCID 59244623HCID 59244623—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 59244850HCID 5924485090%

Reaction Conditions

Temperature100 °C

Reaction Steps

A DMF solution (4 ml) of [tert-butoxycarbonyl-(4-chloro-pyridin-2-yl)-amino]-acetic acid methyl ester (200 mg, 0.667 mmol) obtained in Step A, bis-(4-methoxy-benzyl)-[5-(2-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-pyrimidin-2-yl]-amine (300 mg, 0.556 mmol), palladium acetate (12.5 mg, 0.0556 mmol), S-Phos (46 mg, 0.111 mmol) and potassium phosphate (354 mg, 1.67 mmol) was deaerated under irradiation of ultrasonic wave, followed by stirring at 100° C. for 1 hour under a nitrogen atmosphere. The reaction mixture was cooled to room temperature, and diluted with water, followed by extraction with dichloromethane (30 ml×2). The organic layers were combined, and washed with saturated aqueous sodium chloride solution. After the organic layer was dried over magnesium sulfate, the magnesium sulfate was filtered off, and the filtrate was concentrated under reduced pressure, followed by purification of the residue by silica gel column chromatography (dichloromethane/methanol=50:1), to obtain {[4-(4-{2-[bis-(4-methoxy-benzyl)-amino]-pyrimidin-5-yl}-2-morpholin-4-yl-5,6-dihydro-pyrrolo[2,3-d]pyrimidin-7-yl)-pyridin-2-yl]-tert-butoxycarbonyl-amino}-acetic acid methyl ester as a yellow solid (400 mg, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022205B2
Source datasetuspto-grants-2011_09
ORD IDord-5524c43dbf6c4e6c826d3913441b222b
Source noteuspto-grants-2011_09