Nitrogen → 5-Methoxy-1-methylindazole

HRID 2112152

反応式

HRID 2112152 の反応式
CO[C:3]1[CH:11]=[C:10]2[C:6]([CH:7]=[N:8][NH:9]2)=[CH:5][CH:4]=1.[C:12](=[O:15])([O-])[O-].[K+].[K+].[CH3:18]I.N#N>CN(C=O)C>[CH3:12][O:15][C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:3]=1)[N:9]([CH3:18])[N:8]=[CH:7]2

参加物

6

反応条件

温度
110 °C

実験手順

A solution of 6-methoxy indazole (1t) (5 g, 33.75 mmol; see Tet Lett., 43(15): 2695 (2002)) in DMF (200 mL) was treated with potassium carbonate (6.06 g, 43.87 mmol) at room temperature. After stirring at for 15 minutes, methyl iodide (2.33 mL, 37.12 mmol) was added. The resulting mixture was heated at 110° C. for 18 hours. LC showed minor starting material left. Additional methyl iodide was added (2.33 mL) and stirring continued for an additional 18 hours. LC showed a 2:1 mixture of the N1 to N2 alkylated isomers. The solvent was evaporated in vacuo and the residue taken up in DCM and washed with 1N HCl. The organic layer was filtered through 1PS paper, evaporated in vacuo and purified on the Biotage eluting with 4:3, 3:1 hexane/Et2O. The desired combined fractions (N1 isomer) were evaporated in vacuo to provide the desired product (2t) as a yellow oil (2.57 g; 47%). 1H NMR (400 MHz, CDCl3) 7.38 (d, J=7.8 Hz, 1H), 7.17 (dd, J=7.8, 1.6 Hz, 1H), 7.13 (d, J=1.6 Hz, 1H), 5.19-5.18 (m, 1H), 4.51-4.44 (m, 1H), 4.43-4.36 (m, 1H), 2.53-2.45 (m, 1H), 2.36-2.30 (m, 1H); MS (ESI+) m/z 163 (M+H) detected.

後処理

  1. additionwas added
  2. waitleft
  3. customThe solvent was evaporated in vacuo
  4. washwashed with 1N HCl
  5. filtrationThe organic layer was filtered through 1PS paper
  6. customevaporated in vacuo
  7. custompurified on the Biotage
  8. washeluting with 4:3, 3:1 hexane/Et2O
  9. customwere evaporated in vacuo

出典と根拠

ORDレコード
ord-746c9fddb13c42d5a2b9fb6391c00266
出典データセット
uspto-grants-2009_04
特許番号
US07521447B2

関連ノート

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