HRID641518

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID12665

2-Piperidone

C5H9NO

结构：O=C1CCCN1c1ccc(Oc2ccc3c(c2)CCN(C2CCC2)CC3)nc1

HCID9976892

1-{6-[(3-Cyclobutyl-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl)oxy]pyridin-3-yl}pyrrolidin-2-one

C23H27N3O2

结构：Ic1ccc(Oc2ccc3c(c2)CCN(C2CCC2)CC3)nc1

HCID57440294

未命名化合物

PRODUCTS

生成物

结构：O=C1CCCCN1c1ccc(Oc2ccc3c(c2)CCN(C2CCC2)CC3)nc1

HCID10045991

1-[6-[(3-Cyclobutyl-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl)oxy]-3-pyridinyl]-2-piperidinone

C24H29N3O2

PROCEDURE

实验过程

Example 218 (E218) was prepared from 3-cyclobutyl-7-[(5-iodo-2-pyridinyl)oxy]-2,3,4,5-tetrahydro-1H-3-benzazepine (E207) and 2-piperidinone using the method described for Example 217 (E217); MS (ES+) m/e 392 [M+H]+.