HRID23276

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID68009

Benzaldehyde, 3-fluoro-

C7H5FO

结构：CC(C)(C)OC(=O)N1CC[C@H]2[C@@H](C1)c1cc(N)cc3c1N2CCOC3

HCID86586438

未命名化合物

PRODUCTS

生成物

结构：Fc1cccc(CNc2cc3c4c(c2)[C@@H]2CNCC[C@@H]2N4CCOC3)c1

HCID60071879

未命名化合物

PROCEDURE

实验过程

Using 3-fluorobenzaldehyde and following the procedures described in EXAMPLE 126, tert-butyl (7bR,11aS)-6-amino-1,2,7b,10,11,11a-hexahydro-4H-[1,4]oxazepino[6,5,4-hi]pyrido[4,3-b]indole-9(8H)-carboxylate from EXAMPLE 56, Part B was converted into the title compound of EXAMPLE 132. LRMS (ES)+: 354.4 (M+H)+.