Hydrogen Peroxide → N-{1-[3,5-bis(trifiuoromethyl)phenyl]ethyl}-N-({3-[(cyclopentylmethyl)(ethyl)amino]-6-methoxypyridin-2-yl}methyl)-5-[2-(methylsulfonyl)ethoxy]pyrimidin-2-amine

HRID 1710862Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1710862
[F:1][C:2]([F:46])([F:45])[C:3]1[CH:4]=[C:5]([CH:13]([N:15]([CH2:27][C:28]2[C:33]([N:34]([CH2:37][CH:38]3[CH2:42][CH2:41][CH2:40][CH2:39]3)[CH2:35][CH3:36])=[CH:32][CH:31]=[C:30]([O:43][CH3:44])[N:29]=2)[C:16]2[N:21]=[CH:20][C:19]([O:22][CH2:23][CH2:24][S:25][CH3:26])=[CH:18][N:17]=2)[CH3:14])[CH:6]=[C:7]([C:9]([F:12])([F:11])[F:10])[CH:8]=1.OO.[S:49]([O-:52])([O-])=[O:50].[Na+].[Na+].[C:55](#N)C>[Cl-].[Cl-].[Mo+2](=O)=O>[F:46][C:2]([F:1])([F:45])[C:3]1[CH:4]=[C:5]([CH:13]([N:15]([CH2:27][C:28]2[C:33]([N:34]([CH2:37][CH:38]3[CH2:39][CH2:40][CH2:41][CH2:42]3)[CH2:35][CH3:36])=[CH:32][CH:31]=[C:30]([O:43][CH3:44])[N:29]=2)[C:16]2[N:17]=[CH:18][C:19]([O:22][CH2:23][CH2:24][S:25]([CH3:26])=[O:50])=[CH:20][N:21]=2)[CH3:14])[CH:6]=[C:7]([C:9]([F:10])([F:11])[F:12])[CH:8]=1.[F:46][C:2]([F:1])([F:45])[C:3]1[CH:4]=[C:5]([CH:13]([N:15]([CH2:27][C:28]2[C:33]([N:34]([CH2:37][CH:38]3[CH2:39][CH2:40][CH2:41][CH2:42]3)[CH2:35][CH3:36])=[CH:32][CH:31]=[C:30]([O:43][CH3:44])[N:29]=2)[C:16]2[N:17]=[CH:18][C:19]([O:22][CH2:23][CH2:24][S:49]([CH3:55])(=[O:52])=[O:50])=[CH:20][N:21]=2)[CH3:14])[CH:6]=[C:7]([C:9]([F:11])([F:10])[F:12])[CH:8]=1

Komponenten

7

Edukt 4

HCID 784Hydrogen PeroxideHCID 6342AcetonitrileHCID 24437Sodium SulfiteHCID 25012937N-{1-[3,5-bis(trifluoromethyl)phenyl]ethyl}-N-({3-[(cyclopentylmethyl)(ethyl)amino]-6-methoxypyridin-2-yl}methyl)-5-[2-(methylthio)ethoxy]pyrimidin-2-amine

Produkt 2

HCID 25012936N-{1-[3,5-bis(trifluoromethyl)phenyl]ethyl}-N-({3-[(cyclopentylmethyl)(ethyl)amino]-6-methoxypyridin-2-yl}methyl)-5-[2-(methylsulfinyl)ethoxy]pyrimidin-2-amineAusbeute 10 %HCID 25013093N-{1-[3,5-bis(trifiuoromethyl)phenyl]ethyl}-N-({3-[(cyclopentylmethyl)(ethyl)amino]-6-methoxypyridin-2-yl}methyl)-5-[2-(methylsulfonyl)ethoxy]pyrimidin-2-amineAusbeute 69 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 86628431Dioxomolybdenum(2+) dichlorideKatalysator

Versuchsvorschrift

A solution of N-{1-[3,5-bis(trifluoromethyl)phenyl]ethyl}-N-({3-[(cyclopentylmethyl)(ethyl)amino]-6-methoxypyridin-2-yl}methyl)-5-[2-(methylthio)ethoxy]pyrimidin-2-amine (82 mg, 0.12 mmol) obtained in Example 1 in acetonitrile (3 mL) was added with molybdenum dioxide dichloride (3.6 mg, 0.018 mmol) and 30% aqueous hydrogen peroxide (55 mg, 0.49 mmol), and the mixture was stirred at room temperature for 23 hours. The reaction mixture was added with saturated aqueous sodium sulfite, and the mixture was extracted with chloroform. Then, the organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resulting residue was purified by preparative silica gel thin layer chromatography (hexane:acetone=3:2) to obtain N-{1-[3,5-bis(trifluoromethyl)phenyl]ethyl}-N-({3-[(cyclopentylmethyl)(ethyl)amino]-6-methoxypyridin-2-yl}methyl)-5-[2-(methylsulfinyl)ethoxy]pyrimidin-2-amine (compound of Example 2, 8.4 mg, 10%) as yellow oil, and N-{1-[3,5-bis(trifluoromethyl)phenyl]ethyl}-N-({3-[(cyclopentylmethyl)(ethyl)amino]-6-methoxypyridin-2-yl}methyl)-5-[2-(methylsulfonyl)ethoxy]pyrimidin-2-amine (compound of Example 3, 59.5 mg, 69%) as pale yellow oil.

Aufarbeitung

  1. extractionthe mixture was extracted with chloroform
  2. washThen, the organic layer was washed with saturated brine
  3. dry with materialdried over anhydrous sodium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customThe resulting residue was purified by preparative silica gel thin layer chromatography (hexane:acetone=3:2)

Quellen und Nachweise

ORD-Eintrag
ord-fdf2cd2e1cf8419aba1ff3bdf3905407
Quelldatensatz
uspto-grants-2010_09
Patentnummer
US07790737B2

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