反应详情

2-Methoxybenzylamine (26.1 cc) is added dropwise at a temperature of 10° C. and with stirring to a solution of 10-[(2RS)-1-(1-pyrrolidinyl)-2-propyl]-2-phenothiazinecarbonyl chloride hydrochloride (13.2 g in methylene chloride (125 cc). Stirring is continued for 15 minutes at 10° C. and 16 hours at 20° C. The reaction mixture is washed with distilled water (3×100 cc) and the organic phase is dried over magnesium sulphate, filtered and concentrated to dryness under reduced pressure (30 mm Hg; 4 kPa) at 40° C. The residue is purified by chromatography on a column (height: 64 cm; diameter: 3 cm) of silica gel (0.06-0.2 mm), eluting with ethyl acetate (2 liters) and collecting 200-cc fractions. Fractions 3 to 10 are combined and concentrated to dryness under reduced pressure (30 mm Hg; 4 kPa) at 40° C. to give N-(2-methoxybenzyl)-10-[(2RS)-1-(1-pyrrolidinyl)-2-propyl]-2-phenothiazinecarboxamide (9.3 g) in the form of a white crystalline solid, m.p. 127° C.

1. washThe reaction mixture is washed with distilled water (3×100 cc)
2. dry with materialthe organic phase is dried over magnesium sulphate
3. filtrationfiltered
4. concentrationconcentrated to dryness under reduced pressure (30 mm Hg; 4 kPa) at 40° C
5. customThe residue is purified by chromatography on a column (height: 64 cm; diameter: 3 cm) of silica gel (0.06-0.2 mm)
6. washeluting with ethyl acetate (2 liters)
7. customcollecting 200-cc fractions
8. concentrationconcentrated to dryness under reduced pressure (30 mm Hg; 4 kPa) at 40° C.