4-(3-chloro-1,4-dioxo-1,4-dihydro-naphthalen-2-ylamino)-N-(2-methoxy-phenyl)-benzenesulfonamide → 4-(3-Chloro-1,4-dioxo-1,4-dihydro-naphthalen-2-ylamino)-n-p-tolyl-benzenesulfonamide

HRID 1186666Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1186666
[Cl:1][C:2]1[C:11](=[O:12])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4](=[O:13])[C:3]=1[NH:14][C:15]1[CH:20]=[CH:19][C:18]([S:21]([NH:24][C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=2OC)(=[O:23])=[O:22])=[CH:17][CH:16]=1.Cl[C:34]1C=C(S(N=C2C3C(=CC=CC=3)C(=O)C(Cl)=C2)(=O)=O)SC=1Cl>>[Cl:1][C:2]1[C:11](=[O:12])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4](=[O:13])[C:3]=1[NH:14][C:15]1[CH:20]=[CH:19][C:18]([S:21]([NH:24][C:25]2[CH:26]=[CH:27][C:28]([CH3:34])=[CH:29][CH:30]=2)(=[O:22])=[O:23])=[CH:17][CH:16]=1

Komponenten

3

Versuchsvorschrift

5.2.42 (N-methyl-3-(1-oxo-4-(thiophen-2-ylsulfonylimino)-1,4-dihydronaphthalen-2-ylthio)propanamide (13g) was prepared according to the procedure for 13d except using 4, 5-dichloro-N-(3-chloro-4-oxonaphthalen-1(4H)-ylidene)thiophenesulfonamide (12c) and 3-mercapto-N-methylpropanamide( ) which afforded the title compound 21 mg (32%) as a yellow solid, m.p.: ° C.

Quellen und Nachweise

ORD-Eintrag
ord-ae48ee173de04107b4648345c5315c3f
Quelldatensatz
uspto-grants-2014_03
Patentnummer
US08673910B2

Notizen zur Reaktion

Wird geladen…