Реакция #365187

ord-9ac361d242d04deba14e57bacb2f6bbb

Уравнение реакции

CN1CCC(c2c[nH]c3ccc(OS(=O)(=O)C(F)(F)F)nc23)CC1
O-Trifluoromethanesulfonyl-3-(1-methylpiperidin-4-yl)-5-hydroxy-4-aza-1H-indole
OB(O)c1ccc2ccccc2c1
2-naphthylboronic acid
CN1CCC(c2c[nH]c3ccc(-c4ccc5ccccc5c4)nc23)CC1
title compound
Выход 91.8%
CN1CCC(c2c[nH]c3ccc(-c4ccc5ccccc5c4)nc23)CC1
5-(Naphth-2-yl)-3-(1-Methylpiperidin-4-yl)-4-Aza-1H-Indole
Выход 91.8%

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Методика

O-Trifluoromethanesulfonyl-3-(1-methylpiperidin-4-yl)-5-hydroxy-4-aza-1H-indole (164 mg, 0.450 mmol) and 2-naphthylboronic acid (124 mg, 0.720 mmol) were converted to 141 mg of the title compound by the procedure of Example 3. (91%). MS(FD) m/e 341.8 (M+). EA calculated for C23H23N3: C, 80.94; H, 6.74; N, 12.32. Found: C, 88.11; H, 6.87; N, 12.27.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06358972B1uspto-grants-2002_03