反应 #577197

ord-bc6840b61a2f47df85eb97f708fd6de6

反应方程式

C#CC(O)(c1ccc(N)cc1)c1ccc(F)cc1
1-(4-aminophenyl)-1-(4-fluorophenyl)-2-propyn-1-ol
O=C(c1ccc(F)cc1)c1ccc(F)cc1
4,4′-difluorobenzophenone
Nc1ccc(C(=O)c2ccc(F)cc2)cc1
4-amino-4′-fluorobenzophenone

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

Referring now to FIG. 2, wherein one non-limiting approach to the 1-(4-aminophenyl)-1-(4-fluorophenyl)-2-propyn-1-ol is presented, 4,4′-difluorobenzophenone (7) is reacted with a secondary amine HNR′″R″″ to give the 4-amino-4′-fluorobenzophenone 8, where R′″ and R″″ may be the same as R36 and R37, respectively, as set forth and claimed herein. Acetylide anion, for example, sodium acetylide in acetylene saturated dimethylformamide, is added to the carbonyl of 4-amino-4′-fluorobenzophenone 8 to give, upon aqueous workup, 1-(4-aminophenyl)-1-(4-fluorophenyl)-2-propyn-1-ol 9.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07527754B2uspto-grants-2009_05