反応 #9662

ord-d8bad3c990f7478fabae4a1573965eda

反応方程式

Cl
HCl
CC(C)CCON=O
isoamyl nitrite
Cc1cccc2sc(N)nc12
2-amino-4-methylbenzothiazole
Cc1cccc2sc(Cl)nc12
2-chloro-4-methyl-1,3-benzothiazole
収率 71.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGThe reaction mixture was stirred at rt for 10 minutes
  2. 2
    温度heated at 50° C. for 2.5 h
  3. 3
    温度The reaction mixture was cooled to rt
  4. 4
    抽出The solution was extracted with EtOAc
  5. 5
    洗浄The organic layer was washed with HCl (1.0 M), water, brine
  6. 6
    ろ過filtered
  7. 7
    濃縮concentrated in vacuo
  8. 8
    その他The residue was purified by flash chromatography (Biotage Flash 40M)

実験手順

To a solution containing copper chloride (II) (1.96 g, 14.61 mmol) and tri(ethylene glycol) dimethyl ether (6 mL) in acetonitrile (100 mL) was added isoamyl nitrite (2.14 g, 18.27 mmol), and the reaction mixture was stirred at rt for 30 minutes. To this suspension was added dropwise a solution of 2-amino-4-methylbenzothiazole (2.0 g, 12.18 mmol) in tri(ethylene glycol) dimethyl ether (10 mL). The reaction mixture was stirred at rt for 10 minutes, and then heated at 50° C. for 2.5 h. The reaction mixture was cooled to rt, and then poured cautiously into cold aqueous 6 M HCl (400 mL). The solution was extracted with EtOAc. The organic layer was washed with HCl (1.0 M), water, brine, filtered and concentrated in vacuo. The residue was purified by flash chromatography (Biotage Flash 40M) using 5% ethyl acetate in hexane to afford 2-chloro-4-methyl-1,3-benzothiazole (1.6 g, 71%). 1H NMR (400 MHz, CD2Cl2) δ 2.70 (s, 3H), 7.32 (m, 2H), 7.64 (m, 1H).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07091228B2uspto-grants-2006_08