Triethylamine → HCID 178419362, Verbindung
Reaktionsgleichung
Cl.[Br:2][C:3]1[CH:13]=[CH:12][C:6]([C:7](=[NH:11])OCC)=[CH:5][CH:4]=1.[CH:14]([NH:16][NH2:17])=O.C(N(CC)CC)C>>[Br:2][C:3]1[CH:4]=[CH:5][C:6]([C:7]2[NH:11][CH:14]=[N:16][N:17]=2)=[CH:12][CH:13]=1Komponenten
4
Reaktionsbedingungen
- Temperatur
- 85 °C
Versuchsvorschrift
Ethyl 4-bromobenzimidate hydrochloride (35.6 g, 135 mmol), formic hydrazide (16.16 g, 269 mmol) and triethylamine (75 mL, 538 mmol) were combined in a screw capped flask and heated to 85° C. for 16 h. The solution was condensed under reduced pressure to afford a solid, which was partitioned between water and ethyl acetate (3×), dried over magnesium sulfate and solvent removed under reduced pressure. The resulting solid was sonicated with 20% ethyl acetate in hexanes, filtered and dried to afford the title compound (14.6 g, 65.2 mmol, 48% yield). MS (ESI) m/z 224.1 [M]+, 226.1 [M+2]+.
Aufarbeitung
- customcapped flask
- customcondensed under reduced pressure
- customto afford a solid, which
- customwas partitioned between water and ethyl acetate (3×)
- dry with materialdried over magnesium sulfate and solvent
- customremoved under reduced pressure
- customThe resulting solid was sonicated with 20% ethyl acetate in hexanes
- filtrationfiltered
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-3d15d32d124549d4aa47d04111267bf9
- Quelldatensatz
- uspto-grants-2015_11
- Patentnummer
- US09193692B2
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