tert-Butanol → Tert-butyl (6-methoxypyrazolo[5,1-b][1,3]thiazol-7-yl)carbamate

HRID 1971783

反応式

HRID 1971783 の反応式
[CH3:1][O:2][C:3]1[C:10](C(O)=O)=[C:6]2[S:7][CH:8]=[CH:9][N:5]2[N:4]=1.C([N:16]([CH2:19]C)CC)C.C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=[O:28])C=CC=CC=1.[C:38]([OH:42])([CH3:41])([CH3:40])[CH3:39]>O1CCOCC1>[CH3:1][O:2][C:3]1[C:10]([NH:16][C:19](=[O:28])[O:42][C:38]([CH3:41])([CH3:40])[CH3:39])=[C:6]2[S:7][CH:8]=[CH:9][N:5]2[N:4]=1

参加物

6

実験手順

To a mixture of 6-methoxypyrazolo[5,1-b]thiazole-7-carboxylic acid (300 mg, 1.51 mmol) and 1,4-dioxane (4 mL) were added triethylamine (0.215 mL, 1.54 mmol) and diphenylphosphoryl azide (0.325 mL, 1.51 mmol) while stirring at room temperature, and the mixture was stirred and heated to reflux for 3 hour. After returning the mixture to room temperature, triethylamine (0.631 mL, 4.53 mmol) and tert-butanol (0.289 mL, 3.02 mmol) were added and the mixture was stirred and heated to reflux for 3 hour. After returning the mixture to room temperature, the solvent in the mixture was distilled off under reduced pressure and the residue was purified by silica gel column chromatography (mixture of n-heptane and ethyl acetate: n-heptane/ethyl acetate=1/4) to obtain the title compound (144 mg, 0.535 mmol).

後処理

  1. stirringthe mixture was stirred
  2. temperatureheated
  3. temperatureto reflux for 3 hour
  4. customto room temperature
  5. stirringthe mixture was stirred
  6. temperatureheated
  7. temperatureto reflux for 3 hour
  8. customto room temperature
  9. distillationthe solvent in the mixture was distilled off under reduced pressure
  10. customthe residue was purified by silica gel column chromatography (mixture of n-heptane and ethyl acetate: n-heptane/ethyl acetate=1/4)

出典と根拠

ORDレコード
ord-be7a4a4dee7c42d5bb5b1889f6636f31
出典データセット
uspto-grants-2013_04
特許番号
US08431603B2

関連ノート

読み込み中…