Imidazo[2,1-b]thiazole, 2,3,5,6-tetrahydro-6-phenyl- → Levamisole

HRID 652558

Reaktionsgleichung

Reaktionsgleichung von HRID 652558
[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>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]=1

Komponenten

3

Edukt 1

HCID 3913Imidazo[2,1-b]thiazole, 2,3,5,6-tetrahydro-6-phenyl-

Produkt 1

HCID 26879LevamisoleAusbeute 125,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

A suspension of 31.73 g of L-N-[(4-methoxyphenyl)sulfonyl]-glutamic acid (0.1 mol) in 400 ml of water was stirred and heated till all solid entered solution. Then there were added 20.43 g of tetramisole (0.1 mol) and stirring while heating was continued for a while. The thus obtained homogeneous solution was further stirred for 4 hours while the temperature was allowed to reach room temperature. The precipitate was filtered off, washed with water and dried under vacuo at 50° C., yielding 25.58 g levamisole.L-N-[(4-methoxyphenyl)sulfonyl]glutamic acid (salt) (yield 98.1%) αD20 =-64.2° (c5. 1N HCl); mp. 127.9°-129.4° C.

Aufarbeitung

  1. temperatureheated till all solid
  2. stirringstirring
  3. temperaturewhile heating
  4. stirringThe thus obtained homogeneous solution was further stirred for 4 hours while the temperature
  5. customto reach room temperature
  6. filtrationThe precipitate was filtered off
  7. washwashed with water
  8. customdried under vacuo at 50° C.

Quellen und Nachweise

ORD-Eintrag
ord-72b236fb5e2c451aa9b05a2540a657e6
Quelldatensatz
uspto-grants-1987_06
Patentnummer
US04672126

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