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HRID1398088

反应详情

EQUATION

反应方程式

HRID 1398088 的结构方程式

REACTANTS

反应物

4
结构：O=C1CCOCC1
HCID121599

Tetrahydro-4H-pyran-4-one

C5H8O2

结构：CC(C)(C)OC(=O)NC1CCNCC1
HCID723833

4-(N-Boc-amino)piperidine

C10H20N2O2

结构：O=C1CCC(NC(=O)OCc2ccccc2)CC1
HCID14615292

Benzyl (4-oxocyclohexyl)carbamate

C14H17NO3

结构：CC(C)(C)OC(=O)NN1CCNCC1
HCID21701658

tert-Butyl piperazin-1-ylcarbamate

C9H19N3O2

PRODUCTS

生成物

1
结构：CC(C)(C)OC(=O)N1CCN(C2CCC(NC(=O)OCc3ccccc3)CC2)CC1
HCID57698122

未命名化合物

收率 96%

PROCEDURE

实验过程

The title compound 4.0 g (96%) was obtained in a manner similar to the Manufacturing Example 83 by use of benzyl 4-oxocyclohexylcarbamate and tert-butyl 1-piperazinecarbamate, instead of tetrahydro-4H-pyran-4-one and tert-butyl piperidin-4-ylcarbamate, respectively.