Sodium Carbonate → 1-Benzenesulfonyl-3-isopropyl-4-[3-(5-methanesulfonyl-pyridin-3-yl)-phenyl]-imidazolidin-2-one

HRID 560104

Reaction equation

HRID 560104 reaction equation
[C:1]1([S:7]([N:10]2[CH2:14][CH:13]([C:15]3[CH:20]=[CH:19][CH:18]=[C:17](Br)[CH:16]=3)[N:12]([CH:22]([CH3:24])[CH3:23])[C:11]2=[O:25])(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:26][S:27]([C:30]1[CH:31]=[C:32](B(O)O)[CH:33]=[N:34][CH:35]=1)(=[O:29])=[O:28].C(=O)([O-])[O-].[Na+].[Na+]>O1CCOCC1.O.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2].ClCCl>[C:1]1([S:7]([N:10]2[CH2:14][CH:13]([C:15]3[CH:20]=[CH:19][CH:18]=[C:17]([C:32]4[CH:33]=[N:34][CH:35]=[C:30]([S:27]([CH3:26])(=[O:29])=[O:28])[CH:31]=4)[CH:16]=3)[N:12]([CH:22]([CH3:24])[CH3:23])[C:11]2=[O:25])(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

6

Reactant 3

HCID 10340Sodium CarbonateHCID 441193815-(Methylsulphonyl)pyridine-3-boronic acidHCID 670010961-Benzenesulfonyl-4-(3-bromo-phenyl)-3-isopropyl-imidazolidin-2-one

Product 1

HCID 445482091-Benzenesulfonyl-3-isopropyl-4-[3-(5-methanesulfonyl-pyridin-3-yl)-phenyl]-imidazolidin-2-one

Reagents, catalysts & solvents 2

HCID 178418807HCID 178418807, compoundCatalystHCID 218864351,4-Dioxane--water (1/1)Solvent

Procedure

In analogy to example 1, step 3,1-benzenesulfonyl-4-(3-bromo-phenyl)-3-isopropyl-imidazolidin-2-one (example 12, step 1) was reacted with 5-(methylsulfonyl)-3-pyridineboronic acid in the presence of dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium dichloromethane adduct and sodium carbonate in dioxane/water to give 1-benzenesulfonyl-3-isopropyl-4-[3-(5-methanesulfonyl-pyridin-3-yl)-phenyl]-imidazolidin-2-one as a light yellow oil. MS: 499.9 ([M+H]+)

Sources & evidence

ORD record
ord-00c4d5b050cf4dd8af4ed6cf4aa12d90
Source dataset
uspto-grants-2011_11
Patent number
US08063088B2

Linked notes

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