Reaktion #159671

Reaktionsgleichung

5-chloro-2-(3-phenoxyazetidin-1-yl)nicotinic acid

methyl 4-(1-aminocyclopropyl)benzoate hydrochloride

→

title compound

Ausbeute 117.7%

methyl 4-(1-(5-chloro-2-(3-phenoxyazetidin-1-yl)nicotinamido)cyclopropyl)benzoate

Ausbeute 117.7%

Reaktionsbedingungen

Vorschrift

The title compound (D145) (225 mg) was prepared according to the experimental procedure described in Description 142 starting from 5-chloro-2-(3-phenoxyazetidin-1-yl)nicotinic acid (D101) (140 mg, 0.46 mmol) and methyl 4-(1-aminocyclopropyl)benzoate hydrochloride (D7) (104 mg, 0.40 mmol).

Quelle