تفاعل #7515

ord-a61417b4a55b431fb3b5c4a7891ca0c1

معادلة التفاعل

O
water
CCOC(=O)c1cnc(N2CCc3ccccc32)nc1Cl
ethyl 4-chloro-2-(2,3-dihydro-1H-indol-1-yl)-5-pyrimidinecarboxylate
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
NCc1ccc(F)cc1
4-fluorobenzylamine
CCOC(=O)c1cnc(N2CCc3ccccc32)nc1NCc1ccc(F)cc1
title compound
المردود 81.2%
CCOC(=O)c1cnc(N2CCc3ccccc32)nc1NCc1ccc(F)cc1
ethyl 2-(2,3-dihydro-1H-indol-1-yl)-4-[(4-fluorobenzyl)amino]-5-pyrimidinecarboxylate
المردود 81.2%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةthe mixture was heated
  2. 2
    درجة الحرارةunder reflux for 18 h
  3. 3
    ترشيحThe precipitated crystals were collected by filtration
  4. 4
    غسيلwashed several times with cold water and cold ether
  5. 5
    أخرىdried

الإجراء التجريبي

To a solution of ethyl 4-chloro-2-(2,3-dihydro-1H-indol-1-yl)-5-pyrimidinecarboxylate (607 mg, 2.0 mmol) in isopropanol (5 mL) were added sodium carbonate (424 mg, 4 mmol) and 4-fluorobenzylamine (313 mg, 4 mmol) and the mixture was heated under reflux for 18 h. The reaction mixture was allowed to cool to room temperature and water was added. The precipitated crystals were collected by filtration, washed several times with cold water and cold ether and dried to give the title compound (637 mg, 81%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07087597B1uspto-grants-2006_08