HRID891092

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID222872

4-tert-Butylbenzenesulfonamide

C10H15NO2S

结构：Cc1nn(-c2ccc(CCNC(=O)Oc3ccccc3)cc2)c(C)c1-c1ccccc1

HCID22244550

未命名化合物

PRODUCTS

生成物

结构：Cc1nn(-c2ccc(CCNC(=O)NS(=O)(=O)c3ccc(C(C)(C)C)cc3)cc2)c(C)c1-c1ccccc1

HCID22244522

未命名化合物

PROCEDURE

实验过程

The title compound was prepared according to the procedure described in step 2 of Example 22 from phenyl 2-[4-(3,5-dimethyl-4-phenyl-1H-pyrazol-1-yl)phenyl]ethylcarbamate (step 1 of Example 22) and 4-tert-butyl-benzenesulfonamide: 1H-NMR (CDCl3) δ 7.76 (2H, d, J=8.7 Hz), 7.53-7.24 (11H, m), 6.43 (1H, br.s), 3.54-3.47 (2H, m), 2.87 (2H, t, J=6.6 Hz), 2.33 (3H, s), 2.26 (3H, s), 1.32 (9H, s).

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-fab96d4332584b1389922162ca49931f
来源数据集: uspto-grants-2006_02
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07001917B2
来源说明: uspto-grants-2006_02

反应 SMILES

[CH3:1][C:2]1[C:6]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[C:5]([CH3:13])[N:4]([C:14]2[CH:19]=[CH:18][C:17]([CH2:20][CH2:21][NH:22][C:23](=[O:31])OC3C=CC=CC=3)=[CH:16][CH:15]=2)[N:3]=1.[C:32]([C:36]1[CH:41]=[CH:40][C:39]([S:42]([NH2:45])(=[O:44])=[O:43])=[CH:38][CH:37]=1)([CH3:35])([CH3:34])[CH3:33]>>[C:32]([C:36]1[CH:41]=[CH:40][C:39]([S:42]([NH:45][C:23]([NH:22][CH2:21][CH2:20][C:17]2[CH:16]=[CH:15][C:14]([N:4]3[C:5]([CH3:13])=[C:6]([C:7]4[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=4)[C:2]([CH3:1])=[N:3]3)=[CH:19][CH:18]=2)=[O:31])(=[O:43])=[O:44])=[CH:38][CH:37]=1)([CH3:35])([CH3:33])[CH3:34]