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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186662Generated: October 25, 2026

5-Chlorothiophene-2-Sulfonamide → 5-chloro-N-(3-chloro-4-oxonaphthalen-1(4H)-ylidene)thiophene-2-sulfonamide

https://huagongshe.com/reaction/1186662

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chlorothiophene-2-SulfonamideHCID 1241301—
Reactant(NE)-N-(3-chloro-4-oxonaphthalen-1-ylidene)thiophene-2-sulfonamideHCID 22524852—
Product5-chloro-N-(3-chloro-4-oxonaphthalen-1(4H)-ylidene)thiophene-2-sulfonamideHCID 67330549—

Reaction Steps

5.2.33 5-chloro-N-(3-chloro-4-oxonaphthalen-1(4H)-ylidene)thiophene-2-sulfonamide (12d) was prepared according to the procedure for 12a except using 5-chlorothiophene-2-sulfonamide, which afforded the title compound 320.1 mg (43.0%) as a yellow solid, m.p.: 149-151° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673910B2
Source datasetuspto-grants-2014_03
ORD IDord-860f65e74d6f42dfb026a37e433b9e2b
Source noteuspto-grants-2014_03