Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912149Generated: October 31, 2026

Methyl 4-bromobenzoate → HCID 67385823, compound

https://huagongshe.com/reaction/912149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-bromobenzoateHCID 12081—
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—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 67385823HCID 6738582357.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of bis-(4-methoxy-benzyl)-[5-(2-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-pyrimidin-2-yl]-amine (200 mg, 0.370 mmol), 4-bromobenzoic acid methyl ester (95 mg, 0.444 mmol), palladium acetate (10.0 mg, 0.0444 mmol), S-Phos (36.4 mg, 0.0888 mmol) and potassium phosphate (157 mg, 0.740 mmol) in dimethylformamide (3 ml) was degassed under ultrasonic irradiation, and stirred at 100° C. for 3 hours. To this, water was added, and the precipitate was filtered, which was subsequently dissolved in dichloromethane, and dried over sodium sulfate, followed by concentration under reduced pressure. Purification by silica gel column chromatography (dichloromethane/methanol=200/1) afforded 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)-benzoic acid methyl ester as a yellow powder (143.5 mg, Yield 57%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022205B2
Source datasetuspto-grants-2011_09
ORD IDord-c54e367bb9274121ba76c633250b54df
Source noteuspto-grants-2011_09