Hydrochloric Acid → N-(4-bromo-2-fluorophenyl)-4-methyl-1,3-benzothiazol-2-amine

HRID 9585

반응식

HRID 9585 반응식
Cl[C:2]1[S:3][C:4]2[CH:10]=[CH:9][CH:8]=[C:7]([CH3:11])[C:5]=2[N:6]=1.[Br:12][C:13]1[CH:19]=[CH:18][C:16]([NH2:17])=[C:15]([F:20])[CH:14]=1.Cl>CCCCO>[Br:12][C:13]1[CH:19]=[CH:18][C:16]([NH:17][C:2]2[S:3][C:4]3[CH:10]=[CH:9][CH:8]=[C:7]([CH3:11])[C:5]=3[N:6]=2)=[C:15]([F:20])[CH:14]=1

참가 물질

5

반응 조건

온도
90 °C

실험 절차

To a solution of 2-chloro-4-methyl-1,3-benzothiazole (0.25 g, 1.36 mmol) in n-BuOH (8 mL) was added 4-bromo-2-fluoroaniline (0.52 g, 2.72 mmol) and HCl (4.0 M in dioxane, 0.5 mL). The reaction was heated at 90° C. overnight. Solvent was removed by rotary evaporation and 1 N aqueous HCl was added. The aqueous layer was separated and extracted with EtOAc. The combined organic phases were washed with 1 N aqueous HCl and brine, dried over Na2SO4, filtered, and concentrated in vacuo. The residue was brought up in MeOH and the precipitate was collected by filtration, washed with MeOH, and dried in a vacuum oven to give N-(4-bromo-2-fluorophenyl)-4-methyl-1,3-benzothiazol-2-amine (0.41 g, 89%). 1H NMR (400 MHz, DMSO-d6) δ 2.62 (s, 3H), 7.07 (t, 1H), 7.15 (d, 1H), 7.36 (m, 2H), 7.51 (d, 1H), 8.72 (t, 1H).

후처리

  1. customSolvent was removed by rotary evaporation and 1 N aqueous HCl
  2. additionwas added
  3. customThe aqueous layer was separated
  4. extractionextracted with EtOAc
  5. washThe combined organic phases were washed with 1 N aqueous HCl and brine
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. filtrationthe precipitate was collected by filtration
  10. washwashed with MeOH
  11. customdried in a vacuum oven

출처 및 근거

ORD 기록
ord-3859a45296554bedb58e00427182e1ee
출처 데이터셋
uspto-grants-2006_08
특허 번호
US07091228B2

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