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HRID924396

反应详情

EQUATION

反应方程式

HRID 924396 的结构方程式

REACTANTS

反应物

2
反应SMILES：C1COCCN1
HCID8083

Morpholine

C4H9NO

反应SMILES：CC(C)(C)OC(=O)N[C@H]1CCCN(c2ccncc2NC(=O)c2nc3cc(C=O)ccc3cc2NC(=O)OCc2ccccc2)C1
HCID86726870

未命名化合物

PRODUCTS

产物

1
反应SMILES：Nc1cc2ccc(CN3CCOCC3)cc2nc1C(=O)Nc1cnccc1N1CCC[C@H](N)C1
HCID77844340

未命名化合物

PROCEDURE

实验过程

The title compound was prepared according to the procedure of Example 19 using benzyl (2-{[(4-{(3S)-3-[(tert-butoxycarbonyl)amino]piperidin-1-yl}pyridin-3-yl)amino]carbonyl}-7-formylquinolin-3-yl)carbamate and morpholine as the starting materials to give the title compound in 40% yield. LCMS calc. for C25H32N7O2 (M+H)+: m/z=462.3. Found: 462.2.

WORKUP

后处理

  1. customThe title compound was prepared