HCID 10761567, compound → HCID 131721643, compound

HRID 376864Notes

Reaction equation

HRID 376864 reaction equation
[NH2:1][C:2]([NH2:24])=[N:3][C:4](=[O:23])[C:5]1[C:10]([Cl:11])=[CH:9][C:8]([O:12][C:13]2C=N[CH:16]=[CH:17][CH:18]=2)=[C:7]([S:19]([CH3:22])(=[O:21])=[O:20])[CH:6]=1.[N+:25]([C:28]1C=C(C(C)=CC=1OC1C=NC=CC=1)C(OC)=O)([O-])=O>>[ClH:11].[NH2:24][C:2]([NH2:1])=[N:3][C:4](=[O:23])[C:5]1[C:10]([Cl:11])=[CH:9][C:8]([O:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:28][N:25]=2)=[C:7]([S:19]([CH3:22])(=[O:20])=[O:21])[CH:6]=1

Participants

3

Reactant 2

HCID 10761567HCID 10761567, compoundHCID 19360295HCID 19360295, compound

Product 1

HCID 131721643HCID 131721643, compound

Procedure

N-diaminomethylene-3-methylsulfonyl-4-(3-pyridyloxy)-6-chlorobenzamide, m.p. 215-216°; with methyl 3-nitro-4-(3-pyridyloxy)-6-methylbenzoate,

Sources & evidence

ORD record
ord-d6971ab42d5844359c7cea4b4d3616be
Source dataset
uspto-grants-2000_02
Patent number
US06022883

Reaction notes

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