تفاعل #7009

ord-4c0cc20436e440c9a6f5ae1c9ddc1270

معادلة التفاعل

CCN(C(C)C)C(C)C
Diisopropylethylamine
O=C(O)C1CCN(c2ncccn2)CC1
1-pyrimidin-2-yl-piperidine-4-carboxylic acid
O.On1nnc2ccccc21
1-hydroxybenzotriazole hydrate
CCN=C=NCCCN(C)C.Cl
3-dimethylaminopropyl-3-ethylcarbodiimide hydrochloride
CC(C)CC(=O)NNC(=O)C1CCN(c2ncccn2)CC1
title compound
المردود 46.4%
CC(C)CC(=O)NNC(=O)C1CCN(c2ncccn2)CC1
1-Pyrimidin-2-yl-piperidine-4-carboxylic acid N′-(3-methyl-butyryl)-hydrazide
المردود 46.4%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe solvent was evaporated
  2. 2
    أخرىthe residue was triturated with water

الإجراء التجريبي

The residue was added to a mixture of 1-pyrimidin-2-yl-piperidine-4-carboxylic acid (6.6 g, 31.7 mmol) (see reference U.S. Pat. No. 4,826,843), 1-hydroxybenzotriazole hydrate (4.28 g, 31.7 mmol) and 1-(3-dimethylaminopropyl-3-ethylcarbodiimide hydrochloride (6.09 g, 31.7 mmol) in dichloromethane (50 ml). Diisopropylethylamine (17 ml, 95 mmol) was added and the mixture was stirred for 3 days. The solvent was evaporated and the residue was triturated with water and then with diethyl ether to give the title compound as a white solid (4.49 g).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07084145B2uspto-grants-2006_08