Hydrochloric Acid → HCID 178516641, Verbindung
Reaktionsgleichung
[O-]CC.[Na+].[Cl:5][C:6]1[CH:14]=[CH:13][C:9]([C:10]([NH2:12])=[NH:11])=[CH:8][CH:7]=1.[C:15](OCC)(=[O:22])[CH2:16][C:17](OCC)=[O:18].Cl>C(O)C>[Cl:5][C:6]1[CH:14]=[CH:13][C:9]([C:10]2[N:12]=[C:17]([OH:18])[CH:16]=[C:15]([OH:22])[N:11]=2)=[CH:8][CH:7]=1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 40 °C
Versuchsvorschrift
To sodium ethoxide (48 ml of a 21% wt solution in ethanol diluted with a further 130 ml ethanol) was added 4-chlorobenzamidine (8 g) and diethyl malonate (6.67 ml) and the solution left to stir at 40° C. for 96 hrs. The reaction mixture was subsequently cooled to 5° C. and acidified cautiously to pH 2 using concentrated hydrochloric acid. The solid thus precipitated was filtered, washed with excess cold water, then 50 ml diethyl ether and dried in vacuo yielding the title compound (7.51 g).
Aufarbeitung
- waitthe solution left
- temperatureThe reaction mixture was subsequently cooled to 5° C.
- customThe solid thus precipitated
- filtrationwas filtered
- washwashed with excess cold water
- dry with material50 ml diethyl ether and dried in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-9dd16eab2b6941edbbcb5c059d77f0a9
- Quelldatensatz
- uspto-grants-2009_03
- Patentnummer
- US07501407B2
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