HRID425552

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：O=C1C(c2cc3c(cc2O)CCO3)c2ccccc2N1C(c1ccccc1)c1ccccc1

HCID58872448

未命名化合物

结构：CC1(C)COc2cc(O)c(C3C(=O)N(C(c4ccccc4)c4ccccc4)c4ccccc43)cc21

HCID58872469

未命名化合物

PRODUCTS

生成物

结构：CC1(C)COc2cc(O)c(C3(CO)C(=O)N(C(c4ccccc4)c4ccccc4)c4ccccc43)cc21

HCID58872436

未命名化合物

PROCEDURE

实验过程

Following the procedure as described in PREPARATION 26C, and making non-critical variations to replace 1-(diphenylmethyl)-3-(5-hydroxy-2,3-dihydro-1-benzofuran-6-yl)-1,3-dihydro-2H-indol-2-one with 1-(diphenylmethyl)-3-(6-hydroxy-3,3-dimethyl-2,3-dihydro-1-benzofuran-5-yl)-1,3-dihydro-2H-indol-2-one, the title compound was obtained: MS (ES+) m/z 492.5 (M+1)

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-dcefb05251594fdea6dcb02b83f8ed03
来源数据集: uspto-grants-2012_01
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08106087B2
来源说明: uspto-grants-2012_01

反应 SMILES

C1(C(C2C=CC=CC=2)N2C3C(=CC=CC=3)C(C3C(O)=CC4C[CH2:22][O:23]C=4C=3)C2=O)C=CC=CC=1.[C:34]1([CH:40]([C:63]2[CH:68]=[CH:67][CH:66]=[CH:65][CH:64]=2)[N:41]2[C:49]3[C:44](=[CH:45][CH:46]=[CH:47][CH:48]=3)[CH:43]([C:50]3[C:51]([OH:61])=[CH:52][C:53]4[O:57][CH2:56][C:55]([CH3:59])([CH3:58])[C:54]=4[CH:60]=3)[C:42]2=[O:62])[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1>>[C:63]1([CH:40]([C:34]2[CH:35]=[CH:36][CH:37]=[CH:38][CH:39]=2)[N:41]2[C:49]3[C:44](=[CH:45][CH:46]=[CH:47][CH:48]=3)[C:43]([C:50]3[C:51]([OH:61])=[CH:52][C:53]4[O:57][CH2:56][C:55]([CH3:58])([CH3:59])[C:54]=4[CH:60]=3)([CH2:22][OH:23])[C:42]2=[O:62])[CH:68]=[CH:67][CH:66]=[CH:65][CH:64]=1