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Methane → 5-Chloro-2-[(2-methylphenyl)methyl]-1H-benzimidazole-6-sulfonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methane | HCID 297 | — |
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | 2-(o-Tolyl)acetonitrile | HCID 31155 | — |
| 反応物 | 4,5-Diamino-2-chlorobenzene-1-sulfonamide | HCID 13289688 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 5-Chloro-2-[(2-methylphenyl)methyl]-1H-benzimidazole-6-sulfonamide | HCID 13289710 | — |
反応手順
To 50 ml of 6 N hydrochloric acid was added 11.8 g of 2-amino-4-chloro-5-sulfamylaniline and 10.4 g of 2-methylbenzyl cyanide. The reaction was refluxed for 22 hours and then concentrated in vacuo to a solid which was then added with stirring to 200 ml of 38% ammonium hydroxide. Filtration provided the free base as a semi-gum which was dissolved in 500 ml of methanol. The methanol solution was brought to a boil, charcoal added, and boiling continued for five minutes. Upon cooling, the suspension was filtered through Celite and the filtrate concentrated in vacuo to yield a solid, m.p. 226°-230°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04420487 |
| 出典データセット | uspto-grants-1983_12 |
| ORD ID | ord-cb0c1604acbf44a68236af1dde3cf798 |
| 出典メモ | uspto-grants-1983_12 |