HRID1167960

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：O=C(CCCN1CC=C(n2c(=O)[nH]c3ccccc32)CC1)c1ccc(F)cc1

HCID3168

Droperidol

C22H22FN3O2

HCID137994

4-Hydroxy-2,2,6,6-tetramethylpiperidin-1-yl)oxidanyl

C9H18NO2

PRODUCTS

生成物

结构：CC1(C)CC(O)CC(C)(C)N1[O].O=C(CCCN1CC=C(n2c(=O)[nH]c3ccccc32)CC1)c1ccc(F)cc1

HCID178426855

未命名化合物

PROCEDURE

实验过程

The procedure is performed as for Examples 11 to 13, except that both DHBP and TEMPOL are injected.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-1fd22c4b39844286b3aa732e084756f8
来源数据集: uspto-grants-2003_09
DOI: 10.6084/m9.figshare.5104873.v1
专利: US06620892B1
来源说明: uspto-grants-2003_09

反应 SMILES

[CH2:1]1[C:6]([N:7]2[C:15](=[O:16])[NH:14][C:13]3[C:8]2=[CH:9][CH:10]=[CH:11][CH:12]=3)=[CH:5][CH2:4][N:3]([CH2:17][CH2:18][CH2:19][C:20]([C:22]2[CH:27]=[CH:26][C:25]([F:28])=[CH:24][CH:23]=2)=[O:21])[CH2:2]1.[CH3:29][C:30]1([CH3:40])[N:35]([O:36])[C:34]([CH3:38])([CH3:37])[CH2:33][CH:32]([OH:39])[CH2:31]1>>[CH2:1]1[C:6]([N:7]2[C:15](=[O:16])[NH:14][C:13]3[C:8]2=[CH:9][CH:10]=[CH:11][CH:12]=3)=[CH:5][CH2:4][N:3]([CH2:17][CH2:18][CH2:19][C:20]([C:22]2[CH:27]=[CH:26][C:25]([F:28])=[CH:24][CH:23]=2)=[O:21])[CH2:2]1.[CH3:29][C:30]1([CH3:40])[N:35]([O:36])[C:34]([CH3:38])([CH3:37])[CH2:33][CH:32]([OH:39])[CH2:31]1