Reaktionsgleichung
[CH2:1]([N:3]([CH2:7][CH3:8])[C:4](Cl)=[O:5])[CH3:2].C(Cl)(=O)N.C(NC(Cl)=O)C.CN(C)C(Cl)=O.C([S:28][CH:29]([C:33]1[CH:38]=[CH:37][C:36]([CH:39]2[CH2:44][CH2:43][CH2:42][CH2:41][CH2:40]2)=[C:35]([Cl:45])[CH:34]=1)[C:30]([OH:32])=[O:31])(=O)N.C(NC(SC(C1C=CC(C2CCCCC2)=C(Cl)C=1)C(O)=O)=O)C.CN(C)C(SC(C1C=CC(C2CCCCC2)=C(Cl)C=1)C(O)=O)=O>>[CH2:1]([N:3]([CH2:7][CH3:8])[C:4]([S:28][CH:29]([C:33]1[CH:38]=[CH:37][C:36]([CH:39]2[CH2:40][CH2:41][CH2:42][CH2:43][CH2:44]2)=[C:35]([Cl:45])[CH:34]=1)[C:30]([OH:32])=[O:31])=[O:5])[CH3:2]Komponenten
8
Edukt 7
Produkt 1
Versuchsvorschrift
When diethylcarbamylchloride is replaced in the above procedure by carbamyl chloride (prepared in situ from potassium cyanate and anhydrous hydrogen chloride in anhydrous chloroform), ethylcarbamyl chloride or dimethylcarbamyl chloride, then the products prepared are α-carbamylthio-3-chloro-4-cyclohexylphenylacetic acid, α-ethylcarbamylthio-3-chloro-4-cyclohexylphenylacetic acid or α-dimethylcarbamylthio-3-chloro-4-cyclohexylphenylacetic acid.
Aufarbeitung
- customthe products prepared
Quellen und Nachweise
- ORD-Eintrag
- ord-92c1e3e7e8c844cd84ce9c0ca68eed92
- Quelldatensatz
- uspto-grants-1976_09
- Patentnummer
- US03979428
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