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2-Bromo-5-methylpyridine → 5-methyl-N-(4-(3-(tetrahydro-2H-pyran-4-yl)pyridin-2-yloxy)phenyl)pyridin-2-amine

HRID 473642
ノート
印刷プレビュー

反応式

HRID 473642 の反応式
[O:1]1[CH2:6][CH2:5][CH:4]([C:7]2[C:8]([O:13][C:14]3[CH:20]=[CH:19][C:17]([NH2:18])=[CH:16][CH:15]=3)=[N:9][CH:10]=[CH:11][CH:12]=2)[CH2:3][CH2:2]1.Br[C:22]1[CH:27]=[CH:26][C:25]([CH3:28])=[CH:24][N:23]=1.CC(C)([O-])C.[Na+]>CC(C1C=C(C(C)C)C(C2C(P(C3CCCCC3)C3CCCCC3)=C(OC)C=CC=2OC)=C(C(C)C)C=1)C.C1C=[C-]C(CCN)=CC=1.Cl[Pd+]>[CH3:28][C:25]1[CH:26]=[CH:27][C:22]([NH:18][C:17]2[CH:16]=[CH:15][C:14]([O:13][C:8]3[C:7]([CH:4]4[CH2:3][CH2:2][O:1][CH2:6][CH2:5]4)=[CH:12][CH:11]=[CH:10][N:9]=3)=[CH:20][CH:19]=2)=[N:23][CH:24]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 5642162-Bromo-5-methylpyridineHCID 23676156Sodium t-butoxideHCID 593271274-(3-(tetrahydro-2H-pyran-4-yl)pyridin-2-yloxy)aniline

生成物 1

HCID 593741535-methyl-N-(4-(3-(tetrahydro-2H-pyran-4-yl)pyridin-2-yloxy)phenyl)pyridin-2-amine

試薬・触媒・溶媒 1

HCID 25112666BrettPhos Palladacycle触媒

反応条件

温度
90 °C

実験手順

A glass microwave reaction vessel was charged with 4-(3-(tetrahydro-2H-pyran-4-yl)pyridin-2-yloxy)aniline (0.167 g, 0.619 mmol), 2-bromo-5-methylpyridine (0.0888 g, 0.516 mmol), BrettPHOS precatalyst (8.26 mg, 10.32 μmol), and sodium tert-butoxide (0.124 g, 1.291 mmol). The flask was placed under vacuum then flushed with argon. Dioxane (1.7 mL) was added and the reaction was heated to 90° C. to stir overnight. After cooling to room temperature, the reaction mixture was concentrated and the crude product was adsorbed onto a plug of silica gel and chromatographed through a Biotage pre-packed silica gel column (40S), eluting with a gradient of 10% to 100% EtOAc in hexane, to provide 5-methyl-N-(4-(3-(tetrahydro-2H-pyran-4-yl)pyridin-2-yloxy)phenyl)pyridin-2-amine. MS (ESI, pos. ion) m/z: 362.1 (M+1). IC50 (uM) 0.002387.

後処理

  1. customA glass microwave reaction vessel
  2. customthen flushed with argon
  3. additionDioxane (1.7 mL) was added
  4. temperatureAfter cooling to room temperature
  5. concentrationthe reaction mixture was concentrated
  6. customchromatographed through a Biotage pre-packed silica gel column (40S)
  7. washeluting with a gradient of 10% to 100% EtOAc in hexane

出典と根拠

ORDレコード
ord-f9f3bc2a2e6f4bf5a2202024b9c40f3e
出典データセット
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08637500B2

反応ノート

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