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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258408Generated: November 1, 2026

(NE)-3,4-dichloro-N-(3-chloro-4-oxonaphthalen-1-ylidene)benzenesulfonamide → (NE)-N-[3-(1-methyltetrazol-5-yl)sulfanyl-4-oxonaphthalen-1-ylidene]-4-phenylbenzenesulfonamide

https://huagongshe.com/reaction/1258408

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(NE)-3,4-dichloro-N-(3-chloro-4-oxonaphthalen-1-ylidene)benzenesulfonamideHCID 46908284—
Reactant(NE)-N-[3-(1-methyltetrazol-5-yl)sulfanyl-4-oxonaphthalen-1-ylidene]-4-phenylbenzenesulfonamideHCID 46908285—
ReactantHCID 178527894HCID 178527894—
Product(NE)-N-[3-(1-methyltetrazol-5-yl)sulfanyl-4-oxonaphthalen-1-ylidene]-4-phenylbenzenesulfonamideHCID 4690828529.9%
ProductHCID 178516927HCID 178516927—

Reaction Steps

(E)-N-(3-(1H-1,2,4-triazol-3-ylthio)-4-oxonaphthalen-1(4H)-ylidene)-3,4-dichlorobenzenesulfonamide (13ag) was prepared according to the procedure for 13x except using 12g and 3-mercapto-1,2,4-triazole, affording 27.8 mg (29.9%) title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466157B2
Source datasetuspto-grants-2013_06
ORD IDord-31595a2fa4514d53940fa950cac3371f
Source noteuspto-grants-2013_06