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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258393Generated: November 2, 2026

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

https://huagongshe.com/reaction/1258393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(3-(2-hydroxyethylthio)-4-oxonaphthalen-1(4H)-ylidene)thiophene-2-sulfonamideHCID 67330679—
ReactantN-(4-hydroxy-3-(1-methyl-1H-tetrazol-5-ylthio)naphthalen-1-yl)thiophene-2-sulfonamideHCID 135895396—
ProductN-(4-hydroxy-3-(2-hydroxyethylthio)naphthalen-1-yl)thiophene-2-sulfonamideHCID 46908187—
ProductN-(4-hydroxy-3-(1-methyl-1H-tetrazol-5-ylthio)naphthalen-1-yl)thiophene-2-sulfonamideHCID 13589539653.1%

Reaction Steps

N-(4-hydroxy-3-(2-hydroxyethylthio)naphthalen-1-yl)thiophene-2-sulfonamide (14k) was prepared according to the procedure for 14d except using N-(3-(2-hydroxyethylthio)-4-oxonaphthalen-1(4H)-ylidene)thiophene-2-sulfonamide (13k), which, after purification via flash chromatography (Hex/EtOAc), afforded the title compound 20.3 mg (53.1%) as a grey solid, m.p.: ° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466157B2
Source datasetuspto-grants-2013_06
ORD IDord-756bcc9f546e4df2b821732c1470d85f
Source noteuspto-grants-2013_06