Reaktion #3880

ord-dfc940d1027e4824b71c811ac0ae7fe4

Reaktionsgleichung

COC(=O)CCCCCNC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C
title compound
COC(=O)CCCCCNC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C
t-butoxycarbonyl-N-(6-methoxy-6-oxohexyl)-L-phenylalaninamide
C1COCCO1.Cl
hydrogen chloride dioxane
COC(=O)CCCCCNC(=O)[C@@H](N)Cc1ccccc1.Cl
title compound
COC(=O)CCCCCNC(=O)[C@@H](N)Cc1ccccc1.Cl
N-(6-methoxy-6-oxohexyl)-L-phenylalaninamide monohydrochloride

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    EinengenAfter about 30 min. the solution was concentrated in vacuo to dryness
  2. 2
    Sonstigethe residue triturated thoroughly with diethyl ether
  3. 3
    SonstigeThe solid was collected
  4. 4
    Waschenwashed well with diethyl ether

Vorschrift

To a solution of the title compound of Example 2 (43.1 g, 0.11 mole) in 100 ml of dioxane was added 100 ml of 6M hydrogen chloride/dioxane. After about 30 min. the solution was concentrated in vacuo to dryness and the residue triturated thoroughly with diethyl ether. The solid was collected and washed well with diethyl ether, giving 34.7 g of the title compound, which was used in subsequent reactions without further purification.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04722922uspto-grants-1988_02