HRID1680602

反应详情

EQUATION

反应方程式

HRID 1680602 的结构方程式

PROCEDURE

实验过程

A solution of 1.2 g of nitryltetrafluoroborate in 15 ml of acetonitrile is cooled to 0° C. and a solution of 2.17 g of 5-bromo-2-oxoadamantane [preparation is described in H. W. Geluk, SYNTHESIS, p. 374 (1972)] in 15 ml of acetonitrile is added with rapid stirring and cooling. The reaction mixture is stirred for 30 minutes then poured into water and extracted with diethyl ether. The diethyl ether extract is washed with 5% sodium bicarbonate solution and water and dried over magnesium sulfate. The solvent is removed under reduced pressure to give N-(2-oxoadamantan-5-yl)acetamide. Substitution of an equivalent quantity of N-(2-oxoadamantan-5-yl)acetamide for the methyl 2-oxoadamantane-1-carbamate of Example 57 and substantial repetition of the procedures detailed therein provides methyl L-tyrosyl-D-methionylglycyl-L-phenylalanyl-5-amino-2-adamantanecarboxylate hydrochloride which is represented by the formula ##STR68##

WORKUP

后处理

  1. temperaturecooling
  2. stirringThe reaction mixture is stirred for 30 minutes
  3. extractionextracted with diethyl ether
  4. extractionThe diethyl ether extract
  5. washis washed with 5% sodium bicarbonate solution and water
  6. dry with materialdried over magnesium sulfate
  7. customThe solvent is removed under reduced pressure