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Ammonia → 5-Methyl-2-(3-pyridyl)-thiazole

HRID 1607593
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1607593
[C:1]([CH2:4][NH:5][C:6](=O)[C:7]1[CH:12]=[CH:11][CH:10]=[N:9][CH:8]=1)(=O)[CH3:2].P12(SP3(SP(SP(S3)(S1)=S)(=S)S2)=S)=[S:15].N.C>C1(C)C=CC=CC=1>[CH3:2][C:1]1[S:15][C:6]([C:7]2[CH:8]=[N:9][CH:10]=[CH:11][CH:12]=2)=[N:5][CH:4]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 222AmmoniaHCID 297MethaneHCID 14817Phosphorus sulfide (P2S5)HCID 19612493N-Acetylmethyl-nicotinamide

Produkt 1

HCID 196125135-Methyl-2-(3-pyridyl)-thiazole

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140TolueneLösungsmittel

Versuchsvorschrift

To a solution of 8.0 g (0.045 mol) of 73 in 125 ml of toluene, 10 g (0.045 mol) of P4S10 was added. The suspension was refluxed for 4 h and left at room temperature overnight. The mixture was poured into ice water followed by basification with ammonia. The two-phase system was stirred with charcoal and filtered. The toluene phase was separated and the aqueous phase extracted with 2×100 ml of toluene. The combined organic phases were dried over MgSO4 and evaporated in vacuo leaving a heavy, yellow oil, 88. Yield: 2.3 g (0.013 mol), 29%).

Aufarbeitung

  1. temperatureThe suspension was refluxed for 4 h
  2. filtrationfiltered
  3. customThe toluene phase was separated
  4. extractionthe aqueous phase extracted with 2×100 ml of toluene
  5. dry with materialThe combined organic phases were dried over MgSO4
  6. customevaporated in vacuo
  7. customleaving a heavy, yellow oil, 88

Quellen und Nachweise

ORD-Eintrag
ord-8181380878094ce0ab0506052f44a5f2
Quelldatensatz
uspto-grants-1989_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04866077

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