反应 #312602

ord-319453a6fb2f45b398cd89fed45d81d0

反应方程式

Cl
hydrochloric acid
O=C([O-])[O-].[K+].[K+]
potassium carbonate
Cn1ncc(C(=O)NO)c1SCc1ccccc1
5-benzylthio-1-methylpyrazole-4-carbohydroxamic acid
C=CCBr
allyl bromide
C=CCONC(=O)c1cnn(C)c1SCc1ccccc1
aimed product
收率 82.4%
C=CCONC(=O)c1cnn(C)c1SCc1ccccc1
N-allyloxy-5-benzylthio-1-methylpyrazole-4-carboxylic acid amide
收率 82.4%

反应条件

温度
50°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度After cooling to room temperature
  2. 2
    萃取extracted with ethyl acetate
  3. 3
    洗涤The resulting ethyl acetate solution was washed with water
  4. 4
    干燥dried over anhydrous sodium sulfate
  5. 5
    workup.DISTILLATIONthe solvent was distilled off

实验过程

In a solution of potassium carbonate (1.3 g, 9.4 mmol) in water (10 ml), a solution of 5-benzylthio-1-methylpyrazole-4-carbohydroxamic acid (2.0 g, 7.6 mmol) and allyl bromide (1.1 g, 9.1 mmol) in toluene (10 ml) were added, and stirred at 50° C. for 4 hours. After cooling to room temperature, the mixture was adjusted to pH 1 by adding 35% hydrochloric acid and extracted with ethyl acetate. The resulting ethyl acetate solution was washed with water, dried over anhydrous sodium sulfate, and the solvent was distilled off to obtain the aimed product (1.9 g). Oily substance. Proton nuclear magnetic resonance chemical shift values δ (ppm) (in CDCl3) 3.42 (s, 3H), 3.95 (s, 2H), 4.49 (d, J=6.3 Hz, 2H), 5.33-5.43 (m, 2H), 6.00-6.16 (m, 1H), 6.93-7.00 (m, 2H), 7.21-7.30 (m, 3H), 8.08 (s, 1H), 9.68 (brs, 1H).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07557067B2uspto-grants-2009_07