反応 #2358576

ord-7e5caf38d3914ffba042a378e6c0ee43

反応方程式

O=C(c1cccc(-c2ccc(Oc3ccc(F)cc3)cc2)n1)N1CCNCC1
compound 6
O=C(c1cccc(-c2ccc(Oc3ccc(F)cc3)cc2)n1)N1CCNCC1
(6-(4-(4-fluorophenoxy)phenyl)pyridin-2-yl)(piperazin-1-yl)methanone
CS(=O)(=O)c1cccc(S(=O)(=O)Cl)c1
3-methylsulfonylbenzenesulfonyl chloride
CCN(C(C)C)C(C)C
DIEA
CS(=O)(=O)c1cccc(S(=O)(=O)N2CCN(C(=O)c3cccc(-c4ccc(Oc5ccc(F)cc5)cc4)n3)CC2)c1
compound 8
収率 84.0%
CS(=O)(=O)c1cccc(S(=O)(=O)N2CCN(C(=O)c3cccc(-c4ccc(Oc5ccc(F)cc5)cc4)n3)CC2)c1
(6-(4-(4-fluorophenoxy)phenyl)pyridin-2-yl)(4-((3-(methylsulfonyl)phenyl)sulfonyl)piperazin-1-yl)methanone
収率 84.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他were reacted

実験手順

According to the methodology described in Example 7, compound 6 (100 mg, 0.24 mmol), 3-methylsulfonylbenzenesulfonyl chloride (60 mg, 0.24 mmol), DIEA (0.1 mL, 0.7 mmol) and DCM (5 mL) were reacted to give compound 8 in 84% yield (LC/MS (m/z+H)=596; 1H NMR (CDCl3) δ ppm: 6.8-8.5 (m, 15H); 4.0 (m, 4H); 3.3 (m, 4H); 3.2 (s, 3H)).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09120752B2uspto-grants-2015_09