참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanesulfonic Acid | HCID 6395 | — |
| 반응물 | Benzylamine | HCID 7504 | — |
| 반응물 | 2-Chloro-5-nitrobenzenesulfonamide | HCID 66784 | — |
| 생성물 | 2,5-Diaminobenzenesulfonamide | HCID 21888765 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08101800B2 |
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| 출처 데이터셋 | uspto-grants-2012_01 |
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| ORD ID | ord-d3febb5eec1f41b98f780bc91e009844 |
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| 출처 메모 | uspto-grants-2012_01 |
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