HRID849372

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CC(O)C(CCc1ccccc1)c1ccc(Oc2ccccc2)cc1

HCID19591495

未命名化合物

结构：CC(O)C(CCc1ccccc1)c1ccc(Oc2ccccc2)c(OCc2ccccc2)c1

HCID19591515

未命名化合物

结构：CCOC(=O)CN[C@H](C)[C@H](CCc1ccccc1)c1ccc(Oc2ccccc2)cc1

HCID54550437

未命名化合物

PRODUCTS

生成物

结构：CCOC(=O)CNC(C)C(CCc1ccccc1)c1ccc(Oc2ccccc2)c(OCc2ccccc2)c1

HCID19591456

未命名化合物

PROCEDURE

实验过程

The above identified compound was obtained by carrying out the same reaction as in Example 49(5) and (6) except that instead of (2RS,3SR)-3-(4-phenoxyphenyl)-5-phenylpentan-2-ol used as the starting material in Example 49(2), (2RS,3SR)-3-(3-benzyloxy-4-phenoxyphenyl)-5-phenylpentan-2-ol was used.

WORKUP

后处理

customwas obtained

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-72f00e92efb14b86ae0a0af9cd4742c4
来源数据集: uspto-grants-2000_01
DOI: 10.6084/m9.figshare.5104873.v1
专利: US06011174
来源说明: uspto-grants-2000_01

反应 SMILES

[CH2:1]([O:3][C:4]([CH2:6][NH:7][C@H:8]([CH3:31])[C@@H:9]([C:18]1[CH:23]=[CH:22][C:21]([O:24][C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)=[CH:20][CH:19]=1)[CH2:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)=[O:5])[CH3:2].O(C1C=CC(C(CCC2C=CC=CC=2)C(O)C)=CC=1)C1C=CC=CC=1.[CH2:57]([O:64]C1C=C(C(CCC2C=CC=CC=2)C(O)C)C=CC=1OC1C=CC=CC=1)[C:58]1[CH:63]=[CH:62][CH:61]=[CH:60][CH:59]=1>>[CH2:1]([O:3][C:4]([CH2:6][NH:7][CH:8]([CH3:31])[CH:9]([C:18]1[CH:19]=[CH:20][C:21]([O:24][C:25]2[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=2)=[C:22]([O:64][CH2:57][C:58]2[CH:63]=[CH:62][CH:61]=[CH:60][CH:59]=2)[CH:23]=1)[CH2:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)=[O:5])[CH3:2]