Реакция #155368

ord-ae4dd99dba9341e4a5d8256d9cc01b94

Уравнение реакции

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

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеAfter completion of the reaction the mixture
  2. 2
    Другоеwas evaporated to dryness
  3. 3
    Другоеthe crude product was used without further purification

Методика

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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08821871B2uspto-grants-2014_09