تفاعل #367969

ord-ac01f0377d31454eb32e882eb97bcfb0

معادلة التفاعل

C[C@H](NP(=O)(Cc1ccccc1)Cc1ccccc1)C(=O)N(CC(=O)N1CCC[C@H]1C(=O)O)C1Cc2ccccc2C1
Dibenzylphosphoryl-L-alanyl-N-(2-indanyl)-glycyl-L-proline
N=C(N)NCCC[C@H](N)C(=O)O
L-arginine
C[C@H](NP(=O)(Cc1ccccc1)Cc1ccccc1)C(=O)N(CC(=O)N1CCC[C@H]1C(=O)O)C1Cc2ccccc2C1.N=C(N)NCCC[C@H](N)C(=O)O
dibenzylphosphoryl-L-alanyl-N-(2-indanyl)glycyl-L-proline L-arginine salt
المردود 85.2%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe aqueous solution produced
  2. 2
    workup.ADDITIONwas added
  3. 3
    workup.DISTILLATIONThe solvent was distilled off under reduced pressure
  4. 4
    workup.ADDITIONwater was added
  5. 5
    تجفيفThis water solution was freeze-dried

الإجراء التجريبي

Dibenzylphosphoryl-L-alanyl-N-(2-indanyl)-glycyl-L-proline (0.77 g, 1.2 m mole) was dissolved in ethanol (4 ml), and the aqueous solution produced by dissolving L-arginine (0.25 g, 1.2 m mole) in water (4 ml), was added thereto. The solvent was distilled off under reduced pressure, and then water was added thereto. This water solution was freeze-dried to obtain dibenzylphosphoryl-L-alanyl-N-(2-indanyl)glycyl-L-proline L-arginine salt (0.84 g, yield: 85.2%). This product gave a single spot having an Rf =0.2 for the peptide in free form, and an Rf =0 for arginine, respectively, by thin layer chromatography (developing solvent, acetonitrile:acetic acid=30:1, Colour forming method: spraying of 25% hydrobromic acid and 0.1% ninhydrine, and heating).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04590178uspto-grants-1986_05