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Methylamine → 5-amino-N-methyl-1,3,4-thiadiazole-2-sulfonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methylamine | HCID 6329 | — |
| 反応物 | 5-(Acetylamino)-1,3,4-thiadiazole-2-sulfonyl chloride | HCID 12894451 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 5-amino-N-methyl-1,3,4-thiadiazole-2-sulfonamide | HCID 67483682 | — |
反応手順
Methylamine (2M in THF, 40 mmol) was added to a suspension of 5-acetylamino-1,3,4-thiadiazole-2-sulfonyl chloride (10 mmol) (prepared as described in Bioorg. Med. Chem. 5, 515, 1997) in THF (10 mL) at −20° C. The mixture was stirred at room temperature over night and evaporated to dryness. The crude methylsulfonamide was suspended in EtOH (15 mL) and added 4N HCl in dioxane (15 mL) and heated for 4 h at 80° C. and then cooled to room temperature and evaporated to dryness to give crude 5-amino-1,3,4-thiadiazole-2-sulfonic acid methylamide.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07582769B2 |
| 出典データセット | uspto-grants-2009_09 |
| ORD ID | ord-182dba6a50ef45dc97d03ccfdac3c922 |
| 出典メモ | uspto-grants-2009_09 |