Dimethylcarbamoyl Chloride → alpha-Diethylcarbamylthio-6-methoxy-2-naphthylacetic acid

HRID 1579843

Reaktionsgleichung

Reaktionsgleichung von HRID 1579843
[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:42]=[CH:41][C:40]2[C:35](=[CH:36][CH:37]=[C:38]([O:43][CH3:44])[CH:39]=2)[CH:34]=1)[C:30]([OH:32])=[O:31])(=O)N.C(NC(SC(C1C=CC2C(=CC=C(OC)C=2)C=1)C(O)=O)=O)C.CN(C)C(SC(C1C=CC2C(=CC=C(OC)C=2)C=1)C(O)=O)=O>>[CH2:1]([N:3]([CH2:7][CH3:8])[C:4]([S:28][CH:29]([C:33]1[CH:42]=[CH:41][C:40]2[C:35](=[CH:36][CH:37]=[C:38]([O:43][CH3:44])[CH:39]=2)[CH:34]=1)[C:30]([OH:32])=[O:31])=[O:5])[CH3:2]

Komponenten

8

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-6-methoxy-2-naphthylacetic acid, α-ethylcarbamylthio-6-methoxy-2-naphthylacetic acid or α-dimethylcarbamylthio-6-methoxy-2-naphthylacetic acid.

Aufarbeitung

  1. customthe products prepared

Quellen und Nachweise

ORD-Eintrag
ord-223595e68bfe40c3bf6bc68e0ad04983
Quelldatensatz
uspto-grants-1976_01
Patentnummer
US03931269

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