تفاعل #461286

ord-fea217bdc23f46d0a98aaa52d0692b3f

معادلة التفاعل

CN1CCN(Cc2ccccc2)CC(N)C1
6-amino-1-benzyl-4-methylhexahydro-1H-1,4-diazepine
O=C(O)c1n[nH]c2ccccc12
1H-indazole-3-carboxylic acid
CCN=C=NCCCN(C)C.Cl
1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride
CN1CCN(Cc2ccccc2)CC(NC(=O)c2n[nH]c3ccccc23)C1
title compound
المردود 54.3%
CN1CCN(Cc2ccccc2)CC(NC(=O)c2n[nH]c3ccccc23)C1
N-(1-benzyl-4-methylhexahydro-1H-1,4-diazepin-6-yl)-1H-indazole-3-carboxamide
المردود 54.3%

المذيبات

ظروف التفاعل

درجة الحرارة
25°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلThe reaction mixture is washed successively with water and 10% aqueous sodium hydroxide solution
  2. 2
    تجفيفdried over magnesium sulfate
  3. 3
    أخرىThe solvent is evaporated under reduced pressure
  4. 4
    أخرىthe residue is chromatographed on silica gel with elution of acetone
  5. 5
    workup.ADDITIONFractions containing the title compound
  6. 6
    أخرىevaporated under reduced pressure

الإجراء التجريبي

To a solution of 6-amino-1-benzyl-4-methylhexahydro-1H-1,4-diazepine (1.0 g) in dichloromethane (20 ml), 1H-indazole-3-carboxylic acid (740 mg) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (877 mg) are added, and the resulting mixture is stirred at 25° C. for 2 hours. The reaction mixture is washed successively with water and 10% aqueous sodium hydroxide solution, and dried over magnesium sulfate. The solvent is evaporated under reduced pressure, and the residue is chromatographed on silica gel with elution of acetone. Fractions containing the title compound are pooled and evaporated under reduced pressure to give the title compound (0.9 g) as an oil. The free base thus obtained is converted to the hemifumarate of the title compound in a usual manner, m.p. 192°-194° C. (recrystallized from ethanol).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05166341uspto-grants-1992_11