Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258406Generated: November 2, 2026

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

https://huagongshe.com/reaction/1258406

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(NE)-N-[3-(1-methyltetrazol-5-yl)sulfanyl-4-oxonaphthalen-1-ylidene]-4-phenylbenzenesulfonamideHCID 46908285—
Reactant(NE)-N-(3-chloro-4-oxonaphthalen-1-ylidene)-4-phenylbenzenesulfonamideHCID 58398230—
ReactantHCID 178527894HCID 178527894—
Product(NE)-N-[3-(1-methyltetrazol-5-yl)sulfanyl-4-oxonaphthalen-1-ylidene]-4-phenylbenzenesulfonamideHCID 4690828556.7%
ProductHCID 178516924HCID 178516924—

Reaction Steps

(E)-N-(3-(1H-1,2,4-triazol-3-ylthio)-4-oxonaphthalen-1(4H)-ylidene)biphenyl-4-sulfonamide (13ae) was prepared according to the procedure for 13x except using 12b and 3-mercapto-1,2,4-triazole, affording 53.6 mg (56.7%) title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466157B2
Source datasetuspto-grants-2013_06
ORD IDord-34047e75a66e4514b92115d9d54ec576
Source noteuspto-grants-2013_06