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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353638Generated: October 29, 2026

4-Aminophenylboronic acid → 4-[4-(Methylsulfonylmethyl)-6-morpholin-4-yl-pyrimidine-2-yl]aniline

https://huagongshe.com/reaction/2353638

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Aminophenylboronic acidHCID 2734615—
Reactant2-Methylsulfanyl-4-(methylsulfonylmethyl)-6-morpholin-4-yl-pyrimidineHCID 59379943—
CatalystCuprous 2-thiophenecarboxylateHCID 11194830—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
Product4-[4-(Methylsulfonylmethyl)-6-morpholin-4-yl-pyrimidine-2-yl]anilineHCID 59380039—

Reaction Conditions

Temperature130 °C

Reaction Steps

2-Methylsulfanyl-4-(methylsulfonylmethyl)-6-morpholin-4-yl-pyrimidine (1.00 g, 3.3 mmol), 4-aminophenylboronic acid (904 mg, 6.60 mmol), Copper(I)thiophene-2-carboxylate (1.64 g, 8.58 mmol), Pd(PPh3)4 (153 mg, 0.04 equiv., 0.13 mmol) were added to a microwave vessel and 1,4-Dioxane (20 mL) added. The system was degassed with N2, sealed and heated in a microwave reactor at 130° C. for 1 hour. Upon cooling the reaction was poured into water and the resulting precipitate was collected by filtration and dried under vacuum to afford the title compound as an off-white solid. (988 mg)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750003B2
Source datasetuspto-grants-2010_07
ORD IDord-a90a78aa637941a4bd1fa8f83e4f7ec0
Source noteuspto-grants-2010_07