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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251812Generated: October 25, 2026

N-Bromosuccinamide → N-(4-bromo-3-methyl-5-isoxazolyl)-5-(3-nitrophenyl)thiophene-2-sulfonamide

https://huagongshe.com/reaction/1251812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-BromosuccinamideHCID 9834204—
ReactantN-(3-methyl-5-isoxazolyl)-5-(3-nitrophenyl)thiophene-2-sulfonamideHCID 22998512—
ProductN-(4-bromo-3-methyl-5-isoxazolyl)-5-(3-nitrophenyl)thiophene-2-sulfonamideHCID 23445287—

Reaction Steps

N-(4-bromo-3-methyl-5-isoxazolyl)-5-(3-nitrophenyl)thiophene-2-sulfonamide was prepared in the same manner as described in Example 136C. Reaction of N-(3-methyl-5-isoxazolyl)-5-(3-nitrophenyl)thiophene-2-sulfonamide (328 g, 0.90 mmol) with N-bromosuccinamide (160 mg, 0.90 mmol) gave the final product. A fraction of this material was further purified by preparative HPLC to give the pure sulfonamide as a brown solid, m.p. 132° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06342610B2
Source datasetuspto-grants-2002_01
ORD IDord-33ca9e1047e848b6af1bd83828feebf6
Source noteuspto-grants-2002_01