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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258388Generated: October 25, 2026

N-(3-(1-methyl-1H-tetrazol-5-ylthio)-4-oxonaphthalen-1(4H)-ylidene)thiophene-2-sulfonamide → N-(3-(1-methyl-1H-tetrazol-5-ylthio)-4-oxonaphthalen-1(4H)-ylidene)thiophene-2-sulfonamide

https://huagongshe.com/reaction/1258388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(3-(1-methyl-1H-tetrazol-5-ylthio)-4-oxonaphthalen-1(4H)-ylidene)thiophene-2-sulfonamideHCID 67329899—
Reactant4,5-dichloro-N-(3-chloro-4-oxonaphthalen-1(4H)-ylidene)thiophene-2-sulfonamideHCID 67330668—
Reactant3-mercapto-N-cyclopropylpropanamideHCID 86656567—
ProductN-(3-(1-methyl-1H-tetrazol-5-ylthio)-4-oxonaphthalen-1(4H)-ylidene)thiophene-2-sulfonamideHCID 6732989937%
ProductN-cyclopropyl-3-(1-oxo-4-(thiophen-2-ylsulfonylimino)-1,4-dihydronaphthalen-2-ylthio)propanamideHCID 67330263—

Reaction Steps

N-cyclopropyl-3-(1-oxo-4-(thiophen-2-ylsulfonylimino)-1,4-dihydronaphthalen-2-ylthio)propanamide (13h) was prepared according to the procedure for 13d except using 4,5-dichloro-N-(3-chloro-4-oxonaphthalen-1(4H)-ylidene)thiophenesulfonamide (12c) and 3-mercapto-N-cyclopropylpropanamide ( ), which afforded the title compound 20 mg (37%) as a yellow solid, m.p.: ° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466157B2
Source datasetuspto-grants-2013_06
ORD IDord-eedfdb1f37fe47db887dfc21ce7702eb
Source noteuspto-grants-2013_06