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Thiophosgene → 2-Tert-butyl-6-isothiocyanato-5-(4-methylpiperidin-1-yl)benzothiazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Thiophosgene | HCID 10040 | — |
| 反応物 | Potassium Bicarbonate | HCID 516893 | — |
| 反応物 | 6-Amino-2-tert-butyl-5-(4-methylpiperidin-1-yl)benzothiazole | HCID 19794186 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 2-Tert-butyl-6-isothiocyanato-5-(4-methylpiperidin-1-yl)benzothiazole | HCID 15610362 | — |
反応手順
To a cooled mixture of 2.1 g of 6-amino-2-tert-butyl-5-(4-methylpiperidin-1-yl)benzothiazole and 2.8 g of potassium bicarbonate in 20 ml of chloroform is added dropwise 1.6 g of thiophosgene in 5 ml of chloroform under stirring. The stirring is continued for 2 hours maintaining the temperature at 0°-2° . The solid is filtered and the filtrate is evaporated. The solid thus obtained is dissolved in chloroform and filtered through a silica gel column. The filtrate is evaporated to give 2-tert-butyl-6-isothiocyanato-5-(4-methylpiperidin-1-yl)benzothiazole, melting at 54°-58°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05246927 |
| 出典データセット | uspto-grants-1993_09 |
| ORD ID | ord-6cc07c4d63d84829877b5eb5f5957d9d |
| 出典メモ | uspto-grants-1993_09 |