HCID 10714955, compound → HCID 178504812, compound

HRID 376868Notes

Reaction equation

HRID 376868 reaction equation
[NH2:1][C:2]([NH2:25])=[N:3][C:4](=[O:24])[C:5]1[C:10](C)=[CH:9][C:8]([O:12][C:13]2[CH:14]=[N:15][CH:16]=[C:17]([Cl:19])[CH:18]=2)=[C:7]([S:20]([CH3:23])(=[O:22])=[O:21])[CH:6]=1.CS(C1C=C(C=CC=1OC1(Br)C=CC=CN1)C(OC)=O)(=O)=[O:28]>>[NH2:1][C:2]([NH2:25])=[N:3][C:4](=[O:24])[C:5]1[CH:10]=[CH:9][C:8]([O:12][C:13]2[C:14]([OH:28])=[N:15][CH:16]=[C:17]([Cl:19])[CH:18]=2)=[C:7]([S:20]([CH3:23])(=[O:22])=[O:21])[CH:6]=1

Participants

3

Reactant 2

HCID 10714955HCID 10714955, compoundHCID 86755111HCID 86755111, compound

Product 1

HCID 178504812HCID 178504812, compound

Procedure

N-diaminomethylene-3-methylsulfonyl-4-(5-chloro-3-pyridyloxy)-6-methylbenzamide, m.p. 208-210°; with methyl 3-methylsulfonyl-4-(2-bromo-2-pyridyloxy)benzoate,

Sources & evidence

ORD record
ord-d1c725eabd36427bb640198a91cb159a
Source dataset
uspto-grants-2000_02
Patent number
US06022883

Reaction notes

Loading…