تفاعل #536923

ord-f6f5e58f4ecf4aea858a1cf78a5ac77a

معادلة التفاعل

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}-phenylamino)-propionic acid methyl ester

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىAfter completion of the reaction the mixture
  2. 2
    أخرىwas evaporated to dryness
  3. 3
    أخرىthe crude product was used without further purification

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08486398B2uspto-grants-2013_07