1-Bromo-2-methylpropane → 6-Bromo-5-(2,4-difluorophenoxy)-1-isobutyl-1H-indazole

HRID 909188

反応式

HRID 909188 の反応式
[Br:1][C:2]1[CH:10]=[C:9]2[C:5]([CH:6]=[N:7][NH:8]2)=[CH:4][C:3]=1[O:11][C:12]1[CH:17]=[CH:16][C:15]([F:18])=[CH:14][C:13]=1[F:19].C([O-])([O-])=O.[K+].[K+].[CH2:26](Br)[CH:27]([CH3:29])[CH3:28]>CN(C=O)C>[Br:1][C:2]1[CH:10]=[C:9]2[C:5]([CH:6]=[N:7][N:8]2[CH2:26][CH:27]([CH3:29])[CH3:28])=[CH:4][C:3]=1[O:11][C:12]1[CH:17]=[CH:16][C:15]([F:18])=[CH:14][C:13]=1[F:19]

参加物

5

反応物 3

HCID 65551-Bromo-2-methylpropaneHCID 11430Potassium Carbonate2 回HCID 574187616-Bromo-5-(2,4-difluorophenoxy)-1H-indazole

生成物 1

HCID 574187626-Bromo-5-(2,4-difluorophenoxy)-1-isobutyl-1H-indazole収率 43%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
80 °C

実験手順

6-Bromo-5-(2,4-difluorophenoxy)-1H-indazole (60.0 g, 185 mmol) was dissolved in DMF and treated with K2CO3 (76.5 g, 554 mmol) and with isobutyl bromide (126.4 g, 923 mmol). The mixture was stirred and heated to 80° C. for 16 hours. An additional 15 g of K2CO3 were added and the mixture was vigorously stirred for 24 hours more. The reaction mixture was then cooled to room temperature and filtered. The filtrate was concentrated under reduced pressure and dissolved in ether (1 L). The mixture was washed with 1:5 brine/water (2×600 mL). The aqueous phases were extracted with ether (300 mL) and the combined organics were dried (MgSO4) and concentrated under reduced pressure. The crude product was chromatographed on a Biotage Flash 75 in two batches (about 35 g each) eluting with 5% ethyl acetate in hexanes. The combined purified products yielded 30.1 g of the desired product as a solid (43% yield). MS (ESI+) m/z 381, 383 (M+1, Br pattern) detected; 1H NMR (400 mHz, CDCl3) δ 7.86 (s, 1H), 7.72 (s, 1H), 7.16 (s, 1H), 6.98 (m, 1H), 6.92 (m, 1H), 6.82 (m, 1H), 4.12 (d, 2H), 2.34 (m, 1H), 0.94 (d, 6H).

後処理

  1. stirringthe mixture was vigorously stirred for 24 hours more
  2. temperatureThe reaction mixture was then cooled to room temperature
  3. filtrationfiltered
  4. concentrationThe filtrate was concentrated under reduced pressure
  5. dissolutiondissolved in ether (1 L)
  6. washThe mixture was washed with 1:5 brine/water (2×600 mL)
  7. extractionThe aqueous phases were extracted with ether (300 mL)
  8. dry with materialthe combined organics were dried (MgSO4)
  9. concentrationconcentrated under reduced pressure
  10. customThe crude product was chromatographed on a Biotage Flash 75 in two batches (about 35 g each)
  11. washeluting with 5% ethyl acetate in hexanes
  12. customThe combined purified products

出典と根拠

ORDレコード
ord-a9744326f94b41779374fed51e6ab890
出典データセット
uspto-grants-2011_09
特許番号
US08017641B2

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