HRID486583

反应详情

EQUATION

反应方程式

HRID 486583 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
50 °C

PROCEDURE

实验过程

N-[2-(4,5-Dihydro-7-methoxy-1H-benzo[g]indol-1-yl)ethyl]acetamide (14.5 g) was treated with 50 ml of phosphorus oxychloride under argon and the mixture was stirred at 50° C. for 30 minutes. The cooled mixture was added to 5000 g of ice-water and treated with 500 ml of 28% sodium hydroxide solution. The mixture was extracted once with 1000 ml of methylene chloride and twice with 500 ml of methylene chloride each time, the organic phases were combined, dried with MgSO4 and freed from solvent. The residue, 14.6 g of brown oil, was chromatographed on 220 g of aluminium oxide (neutral, III) with methylene chloride as the eluent. 1.3 g of a total of 10.3 g of crude product were dissolved in a 25-fold amount of ethanol and treated with 1.1 equivalents of a saturated solution of fumaric acid in ethanol. There were obtained 1.2 g (49%) of 5,6,10,11-tetrahydro-3-methoxy-8-methyl-benzo[g]pyrazino[1,2-a]indole fumarate (1:1); m.pt.: 202°-203° C. (dec.).

WORKUP

后处理

  1. extractionThe mixture was extracted once with 1000 ml of methylene chloride and twice with 500 ml of methylene chloride each time
  2. dry with materialdried with MgSO4
  3. customThe residue, 14.6 g of brown oil, was chromatographed on 220 g of aluminium oxide (neutral, III) with methylene chloride as the eluent
  4. dissolution1.3 g of a total of 10.3 g of crude product were dissolved in a 25-fold amount of ethanol