تفاعل #40705

ord-6b46d268ecdb4ada8a7b6d15fb708a7b

معادلة التفاعل

Cl.NC(=O)C(O)C(N)Cc1ccccc1
3-amino-2-hydroxy-4-phenylbutanamide hydrochloride
CCN=C=NCCCN(C)C
1-ethyl-3-(3-dimethylaminopropyl)carbodiimide
Oc1cccc2[nH]nnc12
hydroxylbenzotriazole
O=C(O)c1cccnc1-n1cnc(-c2ccccc2)c1
2-(4-phenyl-1H-imidazol-1-yl)pyridine-3-carboxylic acid
O=C([O-])O.[Na+]
NaHCO3
NC(=O)C(O)C(Cc1ccccc1)NC(=O)c1cccnc1-n1cnc(-c2ccccc2)c1
reddish oil
المردود 37.3%
NC(=O)C(O)C(Cc1ccccc1)NC(=O)c1cccnc1-n1cnc(-c2ccccc2)c1
N-[3-Amino-2-hydroxy-3-oxo-1-(phenylmethyl)propyl]-2-(4-phenyl-1H-imidazol-1-yl)pyridine-3-carboxamide
المردود 37.3%

ظروف التفاعل

درجة الحرارة
2°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGThe mixture was stirred at 0-4° C. for 1 hour
  2. 2
    أخرىat room temperature
  3. 3
    أخرىovernight
  4. 4
    أخرىthe organic phase was separated off
  5. 5
    أخرىDrying
  6. 6
    أخرىevaporating the solvent

الإجراء التجريبي

0.75 g of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC), 0.51 g of hydroxylbenzotriazole (HOBt) and 0.55 ml of triethylamine (Et3N) were successively added to a solution of 1.0 g of 2-(4-phenyl-1H-imidazol-1-yl)pyridine-3-carboxylic acid (3.77 mmol) in 50 ml of dichloromethane at 0-4° C., and the mixture was stirred at 0-4° C. for 1 hour. 0.9 g of 3-amino-2-hydroxy-4-phenylbutanamide hydrochloride (3.9 mmol) and 0.55 ml of Et3N were then added and, after about 5 minutes, a pH of 8-9 was adjusted by adding 0.5 ml of Et3N. The mixture was stirred at 0-4° C. for 1 hour and then at room temperature overnight. 50 ml of saturated NaHCO3 solution were then added to the mixture, and the organic phase was separated off. Drying and evaporating the solvent resulted in 620 mg of a reddish oil, which was reacted further immediately without further purification.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07728012B2uspto-grants-2010_06