Reaktionsgleichung
[CH:1]1[CH:2]=[CH:3][C:4]([CH:7]2[N:14]=[C:13]3[N:9]([CH2:10][CH2:11][S:12]3)[CH2:8]2)=[CH:5][CH:6]=1.Cl.Cl.[OH-].[Na+]>O>[CH:1]1[CH:6]=[CH:5][C:4]([C@@H:7]2[N:14]=[C:13]3[N:9]([CH2:10][CH2:11][S:12]3)[CH2:8]2)=[CH:3][CH:2]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a warmed solution, 40° C., of 24.08 g of tetramisole hydrochloride (0.1 mol) in 113 ml. water adjusted to pH 4 with hydrochloric acid was added dropwise during a period of 50 minutes a suspension containing 15.85 g of L-N-[(4-methoxyphenyl)sulfonyl]glutamic acid (0.05 mol) and 2 g of sodium hydroxide (0.05 mol) in 85 ml of water. The mixture was cooled to 15°-20° C. and additionally stirred during 5 hours. The precipitate was filtered off, washed with water and dried under vacuo at 50° C., yielding 23.55 g of levamisole.L-N-[(4-methoxyphenyl)sulfonyl]glutamic acid (salt) (yield=90.3%); αD20 =-63° (c5, 1N HCl); mp. 127.4°-128.1° C.
Aufarbeitung
- customTo a warmed solution, 40° C.
- additionwas added dropwise during a period of 50 minutes a suspension
- temperatureThe mixture was cooled to 15°-20° C.
- filtrationThe precipitate was filtered off
- washwashed with water
- customdried under vacuo at 50° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-f52767d35d5a4894acefba9be7a5658b
- Quelldatensatz
- uspto-grants-1987_06
- Patentnummer
- US04672126
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