HRID327251

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID7503

Benzyl chloride

C7H7Cl

结构：COC(=O)C(C)(C)Cc1c(Cc2ccc(Cl)cc2)c2ccc(OCc3ccc4ccccc4n3)cc2n1S(=O)(=O)c1ccccc1

HCID18947579

未命名化合物

PRODUCTS

生成物

结构：CC(C)(Cc1c(Cc2ccc(Cl)cc2)c2ccc(OCc3ccc4ccccc4n3)cc2n1Cc1ccccc1)C(=O)O

HCID18947596

未命名化合物

PROCEDURE

实验过程

The title compound was prepared under the conditions described in Step A and Step B of Example 38, but substituting benzyl chloride for the benzenesulfonyl chloride from Example 38 (Step A).

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-d0f78c89cbac4eb9b343c3ba2e57a2e9
来源数据集: uspto-grants-1993_12
DOI: 10.6084/m9.figshare.5104873.v1
专利: US05272145
来源说明: uspto-grants-1993_12

反应 SMILES

[CH2:1](Cl)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C1(S([N:18]2[C:26]3[C:21](=[CH:22][CH:23]=[C:24]([O:27][CH2:28][C:29]4[CH:38]=[CH:37][C:36]5[C:31](=[CH:32][CH:33]=[CH:34][CH:35]=5)[N:30]=4)[CH:25]=3)[C:20]([CH2:39][C:40]3[CH:45]=[CH:44][C:43]([Cl:46])=[CH:42][CH:41]=3)=[C:19]2[CH2:47][C:48]([CH3:54])([CH3:53])[C:49]([O:51]C)=[O:50])(=O)=O)C=CC=CC=1>>[CH2:1]([N:18]1[C:26]2[C:21](=[CH:22][CH:23]=[C:24]([O:27][CH2:28][C:29]3[CH:38]=[CH:37][C:36]4[C:31](=[CH:32][CH:33]=[CH:34][CH:35]=4)[N:30]=3)[CH:25]=2)[C:20]([CH2:39][C:40]2[CH:45]=[CH:44][C:43]([Cl:46])=[CH:42][CH:41]=2)=[C:19]1[CH2:47][C:48]([CH3:54])([CH3:53])[C:49]([OH:51])=[O:50])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1