関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetazolamide | HCID 1986 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 溶媒 | Hydrochloric Acid | HCID 313 | — |
| 生成物 | 5-Amino-1,3,4-thiadiazole-2-sulfonamide | HCID 84724 | 72.9% |
反応手順
Acetazolamide (2.03 g, 9.13 mmol) was combined with 1N HCl (20 mL) and then heated at 100° C. The initial suspension became a clear solution within 3h. After cooling to 0° C. the reaction mixture was carefully neutralized by the addition of solid KOH. Upon standing precipitates had formed and were collected by filtration. The solids were dried under high vacuum to afford 5-amino-[1,3,4]thiadiazole-2-sulfonic acid amide (1.2 g, 70%) as a colorless solid; 1H NMR (DMSO-d6): δ 8.06 (s, 2H), 7.82 (s, 2H). Acetazolamide (2.03 g, 9.13 mmol) was combined with 1 N HCl (20 mL) and then heated at 100° C. The initial suspension became a clear solution within 3h. After cooling to 0° C. A.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08026237B2 |
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| 出典データセット | uspto-grants-2011_09 |
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| ORD ID | ord-5d84373e38b24444bdf252184c130f7c |
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| 出典メモ | uspto-grants-2011_09 |
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