Potassium tert-butoxide → HCID 58155298、化合物
反応式
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([F:19])=[C:6]([C:8]([NH:14][C:15](=[O:18])[CH2:16]Cl)([CH:11]2[CH2:13][CH2:12]2)[CH2:9][OH:10])[CH:7]=1.CC(C)([O-])C.[K+]>C(O)CCC>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([F:19])=[C:6]([C:8]2([CH:11]3[CH2:13][CH2:12]3)[NH:14][C:15](=[O:18])[CH2:16][O:10][CH2:9]2)[CH:7]=1参加物
4
実験手順
In an analogous manner to that described for the preparation of Building block A [e)], the cyclization of (RS)-N-[1-(5-bromo-2-fluoro-phenyl)-1-cyclopropyl-2-hydroxy-ethyl]-2-chloro-acetamide with potassium tert-butoxide in tent-butanol at room temperature overnight yielded the (RS)-5-(5-bromo-2-fluoro-phenyl)-5-cyclopropyl-morpholin-3-one as a yellow oil (2.146 g, 88% of theory). Mass (calculated) C13H13BrFNO2 [314.153]; (found) [M+H]+=314, [M+2-H]+=316.