HRID518667

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CC(C)NC(=O)[C@H]1CC[C@@H](Nc2cc(OCCN3CCCCC3)ncc2N)CC1

HCID178457857

未命名化合物

结构：CC(C)NC(=O)[C@H]1CC[C@@H](Nc2cc(OCCOC3CCCCO3)ncc2[N+](=O)[O-])CC1

HCID178457864

未命名化合物

PRODUCTS

生成物

结构：CC(C)NC(=O)[C@H]1CC[C@@H](Nc2cc(OCCO)ncc2N)CC1

HCID178457865

未命名化合物

PROCEDURE

实验过程

The title compound was synthesized using a method analogous to the preparation of cis-4-(5-amino-2-(2-(piperidin-1-yl)ethoxy)pyridin-4-ylamino)-N-isopropylcyclohexanecarboxamide starting from cis-N-isopropyl-4-(5-nitro-2-(2-(tetrahydro-2H-pyran-2-yloxy)ethoxy)pyridin-4-ylamino)cyclohexanecarboxamide, resulting in the deprotection of the -THP alcohol. MS m/z=337.2 [M+H], calc 336.43 for C17H28N4O3.

WORKUP

后处理

customThe title compound was synthesized