Hydrazine hydrate (1:1) → HCID 66768172, Verbindung

HRID 1959840Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1959840
[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[C:10](=[C:13]1[CH2:17][CH2:16][CH2:15][O:14]1)[C:11]#[N:12].O.[NH2:19][NH2:20]>C(O)C>[NH2:12][C:11]1[C:10]([C:2]2[S:1][C:5]3[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=3[N:3]=2)=[C:13]([CH2:17][CH2:16][CH2:15][OH:14])[NH:19][N:20]=1

Komponenten

4

Edukt 2

HCID 24654Hydrazine hydrate (1:1)HCID 66768211Benzothiazol-2-yl-(dihydrofuran-2-ylidene)-acetonitrile

Produkt 1

HCID 66768172HCID 66768172, VerbindungAusbeute 67 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

The benzothiazol-2-yl-(dihydrofuran-2-ylidene)-acetonitrile (90 mg, 0.37 mmol) prepared above and hydrazine hydrate (25 mg, 0.5 mmol) were refluxed in ethanol (15 mL) for 10 hours. The solvent was evaporated and the resulting residue was triturated with dichloromethane. The solid was isolated by filtration and was then washed with dichloromethane and methanol to yield 60 mg (67%) of the title compound as a cream coloured solid. MS (m/z, ES+): 275.1 (M+1, 100). 1H NMR (300 MHz, ppm, DMSO-d6): δ (ppm), 11.5-12.2 (br s, 1H), 8.00 (d, 1H), 7.86 (d, 1H), 7.77 (t, 2H), 7.29 (t, 1H), 7.00-5.20 (br m, 2H), 4.55 (s, 1H), 3.52 (q, 2H), 2.83 (br s, 2H), 1.84 (q, 2H).

Aufarbeitung

  1. customThe solvent was evaporated
  2. customthe resulting residue was triturated with dichloromethane
  3. customThe solid was isolated by filtration
  4. washwas then washed with dichloromethane and methanol

Quellen und Nachweise

ORD-Eintrag
ord-46346a47c6f7426e8ccb897a907a7013
Quelldatensatz
uspto-grants-2013_04
Patentnummer
US08410272B2

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