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HRID 1165284作成日:2026年10月27日
Hydrochloric Acid → 2-(3'-Amino-4'-sulfophenylamino)-4-chloro-6-(beta-vinylsulfonylethylamino)-1,3,5-triazine
https://huagongshe.com/reaction/1165284
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Cyanuric chloride | HCID 7954 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 2,4-Diaminobenzenesulfonic acid | HCID 66623 | — |
| 反応物 | beta-(beta-Chloroethylsulfonyl)-ethylamine hydrochloride | HCID 19384864 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 2-(3'-Amino-4'-sulfophenylamino)-4-chloro-6-(beta-vinylsulfonylethylamino)-1,3,5-triazine | HCID 19862891 | — |
反応手順
18.8 parts of 1,3-diaminobenzene-4-sulfonic acid are dissolved in 100 parts of water under neutral conditions. This solution is added dropwise in the course of 10 minutes to a mixture of 200 parts of ice and water, 18.5 parts of 2,4,6-trichloro-1,3,5-triazine and 10 parts of 37% hydrochloric acid. The reaction mixture is held at pH 1.5 until the condensation has ended by the continuous addition of 2N sodium hydroxide solution. After the addition of 22.9 parts of β-(β-chloroethylsulfonyl)-ethylamine hydrochloride, the temperature of the reaction mixture is gradually raised from 5° C. to 20° C. while the reaction mixture is initially held at pH 6.5 and then at pH 8.0 by the continuous addition of 2N sodium hydroxide solution. After the condensation and elimination reaction has ended, this reaction mixture is used directly for the acid coupling in Example 4.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04908436 |
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| 出典データセット | uspto-grants-1990_03 |
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| ORD ID | ord-451e6749f9cf49fcab34d87763a7fbfa |
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| 出典メモ | uspto-grants-1990_03 |
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