HRID2244133

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CCN(CC)CCn1nc2c3c(c(C)ccc31)Sc1ccccc1-2

HCID32247

2H-(1)Benzothiopyrano(4,3,2-cd)indazole, 2-(2-(diethylamino)ethyl)-5-methyl-

C20H23N3S

结构：CC(C)(C)c1ccc(S(=O)(=O)N2CCC3=CC(=O)CCC3(Cc3ccc(B4OC(C)(C)C(C)(C)O4)cc3)C2)cc1

HCID59214130

未命名化合物

PRODUCTS

生成物

结构：CC(C)(C)c1ccc(S(=O)(=O)N2CCC3=CC(=O)CCC3(Cc3ccc(N4CCCCC4)cc3)C2)cc1

HCID44442986

未命名化合物

PROCEDURE

实验过程

The following compounds were similarly prepared from 2-(4-t-Butylbenzenesulfonyl)-8a-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)benzyl]-1,3,4,7,8,8a-hexahydro-2H-isoquinolin-6-one (IA-5: Y=4-(B(OC(CH3)2C(CH3)2O)):

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-36ad3073e08d40fd882c0c51304378d6
来源数据集: uspto-grants-2010_03
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07678813B2
来源说明: uspto-grants-2010_03

反应 SMILES

[C:1]([C:5]1[CH:10]=[CH:9][C:8]([S:11]([N:14]2[CH2:23][CH2:22][C:21]3[C:16]([CH2:25][C:26]4[CH:31]=[CH:30][C:29](B5OC(C)(C)C(C)(C)O5)=[CH:28][CH:27]=4)([CH2:17][CH2:18][C:19](=[O:24])[CH:20]=3)[CH2:15]2)(=[O:13])=[O:12])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].CCN(CCN1[N:64]=[C:63]2[C:50]3C(SC4C2=CC=CC=4)=C(C)[CH:53]=[CH:54][C:49]1=3)CC>>[C:1]([C:5]1[CH:6]=[CH:7][C:8]([S:11]([N:14]2[CH2:23][CH2:22][C:21]3[C:16]([CH2:25][C:26]4[CH:27]=[CH:28][C:29]([N:64]5[CH2:53][CH2:54][CH2:49][CH2:50][CH2:63]5)=[CH:30][CH:31]=4)([CH2:17][CH2:18][C:19](=[O:24])[CH:20]=3)[CH2:15]2)(=[O:12])=[O:13])=[CH:9][CH:10]=1)([CH3:4])([CH3:2])[CH3:3]