Reaktion #710535

ord-dd5278d7a5ae40de88fa47dff3132cbf

Reaktionsgleichung

CS(=O)(=O)O
Methanesulfonic acid
CC(C)(C)OC(=O)N1CCC[C@@]1(C)C(=O)O
(S)—N-(tert-butoxycarbonyl)-2-methylproline
CCN(CC)CC
triethylamine
C[C@@]1(C(=O)O)CCCN1
titled compound
C[C@@]1(C(=O)O)CCCN1
(S)-2-methylproline

Lösungsmittel

Reaktionsbedingungen

Temperatur
25°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigea solid was precipitated
  2. 2
    SonstigeThe solid was sufficiently precipitated
  3. 3
    workup.STIRRINGthe solution was stirred at 25° C. for 30 minutes
  4. 4
    workup.STIRRINGfurther stirred at 25° C. for 2 hours
  5. 5
    SonstigeThereafter, the solid was then separated by filtration under reduced pressure
  6. 6
    WaschenThe solid was washed with 1,2-dichloroethane (0.2 mL)
  7. 7
    Sonstigedrying

Vorschrift

Methanesulfonic acid (252 mg, 2.6 mmol) was added to a solution of (S)—N-(tert-butoxycarbonyl)-2-methylproline (500 mg, 2.2 mmol) and 1,2-dichloroethane (2.53 g), and the mixture was stirred at 25° C. for 3 hours. When triethylamine (265 mg, 2.6 mmol) was added thereto, a solid was precipitated. The solid was sufficiently precipitated, and then the solution was stirred at 25° C. for 30 minutes and further stirred at 25° C. for 2 hours. Thereafter, the solid was then separated by filtration under reduced pressure. The solid was washed with 1,2-dichloroethane (0.2 mL), and then was subjected to vacuum drying. Thereby, the titled compound was produced as a white solid (197 mg, yield of 69%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09302980B2uspto-grants-2016_04