HRID724635

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID21878638

2-tert-Butyl-5-chloro-1H-1lambda~6~,2-thiazole-1,1,3(2H)-trione

C7H10ClNO3S

结构：CC1(C)OB(c2ccc(CC(Cc3ccc(-c4ccccc4)cc3)(c3ccccc3)n3nnc4ccccc43)cc2)OC1(C)C

HCID21879401

未命名化合物

PRODUCTS

生成物

结构：CC(C)(C)N1C(=O)C=C(c2ccc(CC(Cc3ccc(-c4ccccc4)cc3)(c3ccccc3)n3nnc4ccccc43)cc2)S1(=O)=O

HCID58746723

未命名化合物

PROCEDURE

实验过程

This compound was prepared according to the procedure of Example 1.1, Step 4, using 4.26-B of Example 2 and 9-A of Example 1.9 as the starting materials. LCMS found for C40H37N4O3S (M+H)+: m/z=653.

WORKUP

后处理

customThis compound was prepared

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-205bd8c7b4984603bb53b2b28e61eb21
来源数据集: uspto-grants-2006_11
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07141596B2
来源说明: uspto-grants-2006_11

反应 SMILES

[C:1]1([C:40]2[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=2)[CH:6]=[CH:5][C:4]([CH2:7][C:8]([N:31]2[C:35]3[CH:36]=[CH:37][CH:38]=[CH:39][C:34]=3[N:33]=[N:32]2)([C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)[CH2:9][C:10]2[CH:15]=[CH:14][C:13](B3OC(C)(C)C(C)(C)O3)=[CH:12][CH:11]=2)=[CH:3][CH:2]=1.[C:46]([N:50]1[C:54](=[O:55])[CH:53]=[C:52](Cl)[S:51]1(=[O:58])=[O:57])([CH3:49])([CH3:48])[CH3:47]>>[N:31]1([C:8]([C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)([CH2:7][C:4]2[CH:3]=[CH:2][C:1]([C:40]3[CH:41]=[CH:42][CH:43]=[CH:44][CH:45]=3)=[CH:6][CH:5]=2)[CH2:9][C:10]2[CH:15]=[CH:14][C:13]([C:52]3[S:51](=[O:58])(=[O:57])[N:50]([C:46]([CH3:49])([CH3:48])[CH3:47])[C:54](=[O:55])[CH:53]=3)=[CH:12][CH:11]=2)[C:35]2[CH:36]=[CH:37][CH:38]=[CH:39][C:34]=2[N:33]=[N:32]1