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HRID 23823作成日:2026年10月26日
Benzenesulfonic acid, 4-(2-(4-(dimethylamino)phenyl)diazenyl)- → 5-Bromo-2-chloro-N-[2-(N-formyl-N-hydroxy-amino)-ethyl]-benzamide
https://huagongshe.com/reaction/23823
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Benzenesulfonic acid, 4-(2-(4-(dimethylamino)phenyl)diazenyl)- | HCID 11037 | — |
| 反応物 | Sodium cyanoborohydride | HCID 5003444 | — |
| 反応物 | Hydrochloride methanol | HCID 21893726 | — |
| 反応物 | 5-bromo-2-chloro-N-(2-hydroxyimino-ethyl)-benzamide | HCID 73987902 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 5-Bromo-2-chloro-N-[2-(N-formyl-N-hydroxy-amino)-ethyl]-benzamide | HCID 22590610 | 35% |
反応手順
To a solution of 5-bromo-2-chloro-N-(2-hydroxyimino-ethyl)-benzamide (2 g, 6.9 mmol) in MeOH (75 mL) under an argon atmosphere at 0° C. was added methyl orange (trace) followed by a saturated solution of MeOH/HCl until a persistent red color was observed. Sodium cyanoborohydride (0.52 g, 8.2 mmol) was dissolved in MeOH (10 mL) and was added sequentially with saturated MeOH/HCl over 0.5 h. The reaction mixture was stirred an additional 2 h and the MeOH was removed in vacuo. The residue was basidified with saturated Na2CO3 and extracted (7×25 mL) with dichloromethane/MeOH (9:1). The combined organic extracts were washed with brine, were dried (Na2SO4) and were concentrated to provide the title compound (0.7 g, 35%) as a white solid. ESMS: M+H=293.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06852882B2 |
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| 出典データセット | uspto-grants-2005_02 |
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| ORD ID | ord-e20624abd66b4a55a6829ef35c4f7191 |
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| 出典メモ | uspto-grants-2005_02 |
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