Acetic Anhydride → Moclobemide

4.0 G. of α-(p-chlorophenyl)-N-(2-morpholinoethyl)-nitrone are heated to 90° C. in 15 ml. of glacial acetic acid and 15 ml. of acetic anhydride for 24 hours. The mixture is then cooled to room temperature, poured into 200 ml. of ice-water and rendered basic with 20% sodium hydroxide solution. Thereafter, the mixture is extracted twice with 100 ml. of methylene chloride each time. The methylene chloride extract is washed with water, dried over sodium sulfate and evaporated. The residue is chromatographed over a silica gel column with a mixture of chloroform and ethanol. The product is recrystallized from isopropanol, and 0.13 g. of p-chloro-N-(2-morpholinoethyl)-benzamide is obtained, which is identical to the product obtained in Example 1.

1. additionpoured into 200 ml
2. extractionThereafter, the mixture is extracted twice with 100 ml
3. extractionThe methylene chloride extract
4. washis washed with water
5. dry with materialdried over sodium sulfate
6. customevaporated
7. customThe residue is chromatographed over a silica gel column with a mixture of chloroform and ethanol
8. customThe product is recrystallized from isopropanol, and 0.13 g

ORD-Eintrag

ord-26a181465b93441a817cdf8b25f8affa

Quelldatensatz

uspto-grants-1980_07

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US04210754