HRID1759266

反应详情

EQUATION

反应方程式

HRID 1759266 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

Nα -(3-benzoylthiopropanoyl)-L-arginine (1 g.) is dissolved with vigorous stirring in a mixture of water (5 ml.) and concentrated ammonia (5 ml.). After one hour, the solution is extracted with ethyl acetate and concentrated to dryness in vacuo. The residue is chromatographed on a column of DEAE Sephadex [anion exchange resin derived from dextran (Mikes, supra, page 328)] (85 ml.) with a buffer of 0.005 M ammonium bicarbonate. The fractions containing the Nα -(3-mercaptopropanoyl)-L-arginine (as indicated by positive thiol and Sakaguchi Reaction) are pooled and lyophilized to remove ammonium bicarbonate, yield 200 mg., m.p. 230° (starts decomposing at 200°).

WORKUP

后处理

  1. extractionthe solution is extracted with ethyl acetate
  2. concentrationconcentrated to dryness in vacuo
  3. customThe residue is chromatographed on a column of DEAE Sephadex [anion exchange resin derived from dextran (Mikes, supra, page 328)] (85 ml.) with a buffer of 0.005 M ammonium bicarbonate
  4. additionThe fractions containing the Nα -(3-mercaptopropanoyl)-L-arginine (as indicated by positive thiol and Sakaguchi Reaction)
  5. customto remove ammonium bicarbonate, yield 200 mg
  6. customm.p. 230° (starts decomposing at 200°)