HRID1366850

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID2736675

2-Chloro-4-(trifluoromethyl)benzenesulfonyl chloride

C7H3Cl2F3O2S

HCID45789790

5-Bromo-6-(trifluoromethyl)pyridin-2-amine

C6H4BrF3N2

HCID57718313

未命名化合物

PRODUCTS

生成物

结构：O=S(=O)(Nc1ccc(Sc2ccc(S(=O)(=O)N3CCOCC3)cc2)c(C(F)(F)F)n1)c1ccc(C(F)(F)F)cc1Cl

HCID57718236

未命名化合物

PROCEDURE

实验过程

Prepared from 2-amino-5-bromo-6-trifluoromethylpyridine and 4-(N -morpholinylsulfonyl)thiophenol according to General Method 11 step 1 followed by reaction with 2-chloro-4-trifluoromethylphenylsulfonyl chloride according to General Method 11 step 2. 1H NMR (CDCl3): 8.31 (1 H, d, J 10 Hz, A-ring CH ortho to SO2NH), 7.45 (1 H, s, A ring CH ortho to CF3 & Cl), 7.65-7.50 & 7.26-7.15 (4 H & 3 H, 2×m, Ar CH's), 3.71-3.61 (4H, m, CH2OCH2), 2.95-2.86 (4H, m, CH2NCH2). Hplc (Luna 2, Gradient 5): rt=6.53 minutes. LC/MS rt=7.06 minutes, 662 (MH+).

WORKUP

后处理

customrt=6.53 minutes
customLC/MS rt=7.06 minutes, 662 (MH+)

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-b7cc77426037460fbe26491744099df9
来源数据集: uspto-grants-2011_02
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07893077B2
来源说明: uspto-grants-2011_02

反应 SMILES

[NH2:1][C:2]1[CH:7]=[CH:6][C:5](Br)=[C:4]([C:9]([F:12])([F:11])[F:10])[N:3]=1.[N:13]1([S:19]([C:22]2[CH:27]=[CH:26][C:25]([SH:28])=[CH:24][CH:23]=2)(=[O:21])=[O:20])[CH2:18][CH2:17][O:16][CH2:15][CH2:14]1.[Cl:29][C:30]1[CH:35]=[C:34]([C:36]([F:39])([F:38])[F:37])[CH:33]=[CH:32][C:31]=1[S:40](Cl)(=[O:42])=[O:41]>>[Cl:29][C:30]1[CH:35]=[C:34]([C:36]([F:38])([F:37])[F:39])[CH:33]=[CH:32][C:31]=1[S:40]([NH:1][C:2]1[CH:7]=[CH:6][C:5]([S:28][C:25]2[CH:24]=[CH:23][C:22]([S:19]([N:13]3[CH2:14][CH2:15][O:16][CH2:17][CH2:18]3)(=[O:21])=[O:20])=[CH:27][CH:26]=2)=[C:4]([C:9]([F:12])([F:11])[F:10])[N:3]=1)(=[O:42])=[O:41]