Phosphorus oxychloride → [5-(3-Chloro-2,6-dimethoxy-phenyl)-[1,3,4]thiadiazol-2-yl]-cyclohexyl-amine

HRID 1244770

Reaktionsgleichung

Reaktionsgleichung von HRID 1244770
[Cl:1][C:2]1[C:3]([O:13][CH3:14])=[C:4]([C:8]([O:11][CH3:12])=[CH:9][CH:10]=1)[C:5](O)=O.[NH2:15][NH:16][C:17]([NH2:19])=[S:18].O=P(Cl)(Cl)Cl.C([O-])(O)=O.[Na+]>O1CCOCC1>[Cl:1][C:2]1[C:3]([O:13][CH3:14])=[C:4]([C:5]2[S:18][C:17]([NH:19][CH:2]3[CH2:3][CH2:4][CH2:8][CH2:9][CH2:10]3)=[N:16][N:15]=2)[C:8]([O:11][CH3:12])=[CH:9][CH:10]=1

Komponenten

6

Edukt 4

HCID 24813Phosphorus oxychlorideHCID 516892Sodium BicarbonateHCID 6121993-Chloro-2,6-dimethoxybenzoic acidHCID 2723789Thiosemicarbazide

Produkt 1

HCID 21920332[5-(3-Chloro-2,6-dimethoxy-phenyl)-[1,3,4]thiadiazol-2-yl]-cyclohexyl-amineAusbeute 28,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 312751,4-DioxaneLösungsmittel

Reaktionsbedingungen

Temperatur
95 °C

Versuchsvorschrift

To a mixture of 3-chloro-2,6-dimethoxybenzoic acid (2.3 mmol, 500 mg), thiosemicarbazide (5b) (2.3 mmol, 399 mg) in anhydrous dioxane (10 mL) at 70° C. to 80° C., POCl3 (2.3 mmol, 215 μL) was added, and the mixture was warmed at 95° C. for 5 hours. The solvent was removed by distillation under reduced pressure to give a crude material which was basified at pH 8-7 with a saturated solution of NaHCO3. The precipitate obtained was collected by filtration, washed with water, and dried under vacuum. The solid was subjected to flash chromatography eluting with ethyl acetate/cyclohexane to give 115 mg of the title compound. Yield: 14%.

Aufarbeitung

  1. customThe solvent was removed by distillation under reduced pressure
  2. customto give a crude material which
  3. customThe precipitate obtained
  4. filtrationwas collected by filtration
  5. washwashed with water
  6. customdried under vacuum
  7. washeluting with ethyl acetate/cyclohexane

Quellen und Nachweise

ORD-Eintrag
ord-2e62bdf86a6245e98d2b2df36ff3b878
Quelldatensatz
uspto-grants-2006_10
Patentnummer
US07122565B2

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