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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353654Generated: October 31, 2026

Water → (4-{4-Morpholin-4-yl-6-[(phenylsulfonyl)methyl]pyrimidin-2-yl}phenyl)amine

https://huagongshe.com/reaction/2353654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 2734620—
Reactant4-{2-Chloro-6-[(phenylsulfonyl)methyl]pyrimidin-4-yl}morpholineHCID 59380090—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
Solvent1,2-DimethoxyethaneHCID 8071—
Product(4-{4-Morpholin-4-yl-6-[(phenylsulfonyl)methyl]pyrimidin-2-yl}phenyl)amineHCID 59380186—

Reaction Conditions

Temperature90 °C

Reaction Steps

4-{2-Chloro-6-[(phenylsulfonyl)methyl]pyrimidin-4-yl}morpholine (3.3 g, 9.33 mmol) was dissolved in a solution of 18% DMF in a mixture of 7:3:2 dimethoxyethane:water:ethanol (36 mL). [4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]amine (3.07 g, 13.99 mmol), 2M sodium carbonate solution (12 mL) and dichlorobis(triphenylphosphine) palladium catalyst (328 mg, 0.47 mmol) were then added and the reaction refluxed at 90° C. for 2 hours under a nitrogen atmosphere. The reaction was allowed to cool to room temp then partitioned between ethyl acetate (20 mL) and water (20 mL). The organics were dried over magnesium sulphate, filtered and concentrated in vacuo. The crude oil was dissolved in DCM and filtered to remove insoluble material. A beige solid precipitated from the filtrates and the filtrates were filtered again. The solid was analysed and found to be the desired material (2.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750003B2
Source datasetuspto-grants-2010_07
ORD IDord-988770d518634c77a5260894e1c3e4b0
Source noteuspto-grants-2010_07