戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 424169作成日:2026年10月26日

Methanesulfonic Acid → 2,5-Diaminobenzenesulfonamide

https://huagongshe.com/reaction/424169

反応式

関与物質

役割名称HCID仕込み量
反応物Methanesulfonic AcidHCID 6395—
反応物BenzylamineHCID 7504—
反応物2-Chloro-5-nitrobenzenesulfonamideHCID 66784—
生成物2,5-DiaminobenzenesulfonamideHCID 21888765—

反応手順

The 2-chloro-5-nitro-benzenesulfonamide intermediate (prepared as described in scheme 14) can be treated with a benzylic amine, such as benzylamine, to displace the chloro moiety. Hydrogenation under standard conditions in the presence of an acid (e.g., methanesulfonic acid) can be used to remove the benzylic group and to reduce the nitro group at the same time to afford the 2,5-diamino-benzenesulfonamide intermediate as a salt. Alternatively, the 2,5-diamino-benzenesulfonamide salt can be prepared by reduction of the 2-amino-5-nitro-benzenesulfonamide (prepared as described in schemes 14 and 15) under standard hydrogenation conditions in the presence of an acid (e.g., methanesulfonic acid). Subsequent reaction with methanesulfonyl chloride affords the desired 2-amino-5-methanesulfonylamino-benzenesulfonamide intermediate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08101800B2
出典データセットuspto-grants-2012_01
ORD IDord-d3febb5eec1f41b98f780bc91e009844
出典メモuspto-grants-2012_01