Réaction #155368

ord-ae4dd99dba9341e4a5d8256d9cc01b94

Équation de réaction

CNc1ccc(C(=O)N(CCC(=O)OC)c2ccccc2)cc1N
1b
CNc1ccc(C(=O)N(CCC(=O)OC)c2ccccc2)cc1N
3-[(3-Amino-4-methylamino-benzoyl)-phenyl-amino]-propionic acid methyl ester
N#Cc1ccc(NCC(=O)O)cc1
N-(4-cyano-phenyl)-glycine
O=C(n1ccnc1)n1ccnc1
CDI
CNc1ccc(C(=O)N(CCC(=O)OC)c2ccccc2)cc1NC(=O)CNc1ccc(C#N)cc1
3-({3-[2-(4-Cyano-phenylamino)-acetylamino]-4-methylamino-benzoyl}-phenyl-amino)-propionic acid methyl ester

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreAfter completion of the reaction the mixture
  2. 2
    Autrewas evaporated to dryness
  3. 3
    Autrethe crude product was used without further purification

Mode opératoire

The product of 1b (23.2 mmol) and N-(4-cyano-phenyl)-glycine (23.2 mmol) were coupled with CDI (23.2 mmol) in dry THF at room temperature. After completion of the reaction the mixture was evaporated to dryness and the crude product was used without further purification.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08821871B2uspto-grants-2014_09