反应详情
EQUATION
反应方程式
REACTANTS
反应物
4-Pyridinemethanamine
C6H8N2
3-Nitropyridine
C5H4N2O2
(6-methylpyridin-2-yl)methanamine
C7H10N2
(4-(trifluoromethyl)pyridin-2-yl)methanamine
C7H7F3N2
未命名化合物
4-Phenyl-2-pyridinemethanamine
C12H12N2
未命名化合物
未命名化合物
未命名化合物
未命名化合物
未命名化合物
未命名化合物
1-(3-Chloropyridin-2-yl)methanamine
C6H7ClN2
1-(4-Methoxypyridin-2-yl)methanamine
C7H10N2O
PRODUCTS
生成物
PROCEDURE
实验过程
Similarly, following the above procedure but replacing the 4-aminomethylpyridine as used therein with an equal molar proportion of 2-aminomethyl-6-methylpyridine, 2-(2-aminoethyl)-5-ethylpyridine, 3-amino-5-(aminomethyl)-2-methylpyridine, 2-(aminomethyl)-3-chloropyridine, 2-(aminomethyl)-4-phenylpyridine, 2-(aminomethyl)-4-benzylpyridine, 2-(aminomethyl)-4-methoxypyridine, 2-(aminomethyl)-4-methylthiopyridine, 2-aminomethyl)-3-nitropyridine, 2-(aminomethyl)-3-ethylaminopyridine, 2-(aminomethyl)-3-diethylaminopyridine, 2-(aminomethyl)-4-acetylaminopyridine, and 2-(aminomethyl)-4-trifluoromethylpyridine, respectively, all of which may be prepared by reduction of the corresponding nitrile of formula (IVC) according to the method of Sculley, et al., supra., there is obtained
WORKUP
后处理
- custom, there is obtained