関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | 3-amino-N-ethylpiperidine | HCID 98094 | — |
| 反応物 | 4-(7-Chloro-4-cinnolinylamino)benzenesulphonylchloride hydrochloride | HCID 21273956 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | HCID 13537214 | HCID 13537214 | — |
反応手順
3-Amino-1-ethylpiperidine (0.4 ml) in chloroform (15 ml) was treated with anhydrous sodium carbonate (2.94 g) in water (15 ml) and cooled to 3° C. The mixture was vigorously stirred and treated with 4-(7-chloro-4-cinnolinylamino)benzenesulphonylchloride hydrochloride (1.0 g). The dark orange mixture was stirred at 3° C. for 15 minutes, then at room temperature for 45 minutes. During this period the colour lightened considerably. The chloroform layer was separated and dried over magnesium sulphate. The residue on evaporation solidified when triturated with methanol, to give the title compound (0.5 g), m.p. 213°-15° C. (with decomposition).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04640920 |
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| 出典データセット | uspto-grants-1987_02 |
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| ORD ID | ord-f64cd5b988b14d4f8e6425d0bb08320b |
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| 出典メモ | uspto-grants-1987_02 |
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