Реакция #467733

ord-559d4f209c15476c853aa4fa79fbaa46

Уравнение реакции

OB(O)c1ccc2ccccc2c1
naphthalene-2-boronic acid
CCC1CC(OS(=O)(=O)C(F)(F)F)=CCN1C(=O)Oc1ccccc1
1-phenoxycarbonyl-2-ethyl-4-trifluoromethanesulfonyloxy-1,2,3,6-tetrahydropyridine
CCC1CC(c2ccc3ccccc3c2)=CCN1C(=O)Oc1ccccc1
desired compound
Выход 75.3%
CCC1CC(c2ccc3ccccc3c2)=CCN1C(=O)Oc1ccccc1
1-phenoxycarbonyl-2-ethyl-4-(naphth-2-yl)-1,2,3,6-tetrahydropyridine
Выход 75.3%

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Методика

Beginning with 3.62 gm (21.1 mMol) naphthalene-2-boronic acid and 5.70 gm (15.0 mMol) 1-phenoxycarbonyl-2-ethyl-4-trifluoromethanesulfonyloxy-1,2,3,6-tetrahydropyridine, 4.04 gm (75%) of the desired compound were prepared substantially as described in EXAMPLE 11.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06303627B1uspto-grants-2001_10