o-Anisohydrazide → N-cyclopropyl-2-(2-methoxybenzoyl)-hydrazinecarboxamide
Reaktionsgleichung
[CH:1]1([N:4]=[C:5]=[O:6])[CH2:3][CH2:2]1.[CH3:7][O:8][C:9]1[CH:18]=[CH:17][CH:16]=[CH:15][C:10]=1[C:11]([NH:13][NH2:14])=[O:12]>C1COCC1>[CH:1]1([NH:4][C:5]([NH:14][NH:13][C:11](=[O:12])[C:10]2[CH:15]=[CH:16][CH:17]=[CH:18][C:9]=2[O:8][CH3:7])=[O:6])[CH2:3][CH2:2]1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
250 mg (3.01 mmol) of cyclopropyl isocyanate, dissolved in 3 ml THF, are added dropwise to 500 mg (3.01 mmol) of 2-methoxybenzoic acid hydrazide, dissolved in 7 ml THF, and the mixture stirred overnight at room temperature. The resulting precipitate is filtered off, washed with diethyl ether and dried in vacuo. 709 mg (94% of theory) of the target compound are thus obtained.
Aufarbeitung
- filtrationThe resulting precipitate is filtered off
- washwashed with diethyl ether
- customdried in vacuo
- custom709 mg (94% of theory) of the target compound are thus obtained
Quellen und Nachweise
- ORD-Eintrag
- ord-d9ad31ea3884469a9d9f0c0f818bb790
- Quelldatensatz
- uspto-grants-2011_12
- Patentnummer
- US08084481B2
Notizen zur Reaktion
Wird geladen…