反応 #155368

ord-ae4dd99dba9341e4a5d8256d9cc01b94

反応方程式

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

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他After completion of the reaction the mixture
  2. 2
    その他was evaporated to dryness
  3. 3
    その他the crude product was used without further purification

実験手順

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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08821871B2uspto-grants-2014_09