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HRID1591432

反应详情

EQUATION

反应方程式

HRID 1591432 的结构方程式

REACTANTS

反应物

2
结构：CC(C)(C)OC(=O)NC(C)(C)C(=O)O
HCID2733845

N-((1,1-Dimethylethoxy)carbonyl)-2-methyl-alanine

C9H17NO4

结构：NC1CCc2ccccc2NC1=O
HCID4434433

3-Amino-1,3,4,5-tetrahydro-2H-1-benzazepin-2-one

C10H12N2O

PRODUCTS

生成物

1
结构：CC(C)(C)OC(=O)NC(C)(C)C(=O)NC1CCc2ccccc2NC1=O
HCID21836680

未命名化合物

PROCEDURE

实验过程

Prepared from 2-(t-butoxycarbonylamino)-2-methylpropanoic acid and 3-amino-2,3,4,5-tetrahydro-1H-[1]benzazepin-2-one (Example 1, Step A) by the procedure described in Example 25, Step A. 1H NMR (200 MHz, CDCl3): 1.38 *s,12H), 1.44 (s,3H), 1.90 (m,1H), 2.5-3.0 (m,3H), 4.45 (m,1H), 5.10 (s,1H), 6.97 (m,1H), 7.20 (m,3H), 8.45 (s,1H).