関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Riluzole | HCID 5070 | — |
| 反応物 | Sodium Iodide | HCID 5238 | — |
| 反応物 | N-(2-Chloroethyl)acetamide | HCID 81815 | — |
| 溶媒 | Methyl Ethyl Ketone | HCID 6569 | — |
| 生成物 | 3-(2-Acetamidoethyl)-2-imino-6-trifluoromethoxybenzothiazoline | HCID 3076411 | 21.1% |
反応手順
2-Amino-6-trifluoromethoxybenzothiazole (9.4 g), N-(2-chloroethyl)acetamide (9.7 g) and sodium iodide (13.5 g) in methyl ethyl ketone (30 cc) are heated for 40 hours to boiling. After cooling to a temperature in the region of 20° C., the reaction medium is added to distilled water (200 cc), treated with 1N sodium hydroxide (40 cc) and then extracted with ethyl acetate (200 cc). After drying over magnesium sulphate and then concentration to dryness at 40° C. under reduced pressure (20 mm Hg; 2.7 kPa), the residue is purified by chromatography on a silica column with a mixture of ethyl acetate and methanol (90:10 by volume) as eluent. 3-(2-Acetamidoethyl)-2-imino-6-trifluoromethoxybenzothiazoline (2.7 g) is obtained, which product is converted to a hydrochloride subliming at about 180° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04980356 |
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| 出典データセット | uspto-grants-1990_12 |
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| ORD ID | ord-5adc69eb76704e68ba0a32ca3e20db64 |
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| 出典メモ | uspto-grants-1990_12 |
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