Imidazole → (S)-(2-Iodo-1-methyl-ethyl)-carbamic acid tert-butyl ester

HRID 1158744

反応式

HRID 1158744 の反応式
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.N1C=CN=C1.[I:25]I.[C:27]([NH:34][C@H:35]([CH2:37]O)[CH3:36])([O:29][C:30]([CH3:33])([CH3:32])[CH3:31])=[O:28]>C(Cl)Cl>[I:25][CH2:37][C@@H:35]([NH:34][C:27](=[O:28])[O:29][C:30]([CH3:33])([CH3:32])[CH3:31])[CH3:36]

参加物

6

反応条件

温度
0 °C

実験手順

PS-triphenylphosphine (2.5 mmol/g, 1.3 g, 3.3 mmol) was suspended in methylene chloride (12 mL). Imidazole (225 mg, 3.3 mmol) was added and the mixture was cooled to 0° C. in an ice-water bath. To the cooled mixture was added iodine (838 mg, 3.3 mmol), and the resulting mixture was warmed to room temperature, stirred 10 minutes and recooled to 0° C. Boc-L-alaninol (463 mg, 2.64 mmol) in methylene chloride (3 mL) was added over several minutes. The resulting mixture was stirred at 0° C. for 1 hour, warmed to room temperature and stirred 2 h. The mixture was filtered. The solids collected were washed thoroughly with ethyl acetate. The filtrate washed with dilute aqueous HCl (3%), sodium thiosulfate (1 M), saturated aqueous sodium bicarbonate and brine. The extracts were then dried over magnesium sulfate, filtered and concentrated under reduced pressure. The crude tert-butyl [(1S)-2-iodo-1-methylethyl]carbamate (xxvii) was obtained as a yellow oil and used without further purification. 1H NMR (300 MHz, CDCl3): δ 3.34-3.56 (m, 2H), 3.27 (dd, J=3.7, 9.8 Hz, 1H), 1.43 (s, 9H), 1.18 (d, J=6.7 Hz, 3H).

後処理

  1. temperaturethe resulting mixture was warmed to room temperature
  2. customrecooled to 0° C
  3. stirringThe resulting mixture was stirred at 0° C. for 1 hour
  4. temperaturewarmed to room temperature
  5. stirringstirred 2 h
  6. filtrationThe mixture was filtered
  7. customThe solids collected
  8. washwere washed thoroughly with ethyl acetate
  9. washThe filtrate washed with dilute aqueous HCl (3%), sodium thiosulfate (1 M), saturated aqueous sodium bicarbonate and brine
  10. dry with materialThe extracts were then dried over magnesium sulfate
  11. filtrationfiltered
  12. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-a5fc0d0c8c6540c292140d8b1598f130
出典データセット
uspto-grants-2010_10
特許番号
US07812018B2

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