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Butyl isocyanate → N-(Butylcarbamoyl)-3-methylthiophene-2-sulfonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Butyl isocyanate | HCID 8110 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 3-Methylthiophene-2-sulfonamide | HCID 341083 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | N-(Butylcarbamoyl)-3-methylthiophene-2-sulfonamide | HCID 13203354 | — |
反応手順
To 150 ml of acetone and 3-methyl-2-thiophenesulfonamide was added 11 g of n-butyl isocyanate and 14 g of anhydrous potassium carbonate. After stirring at ambient temperature for 24 hours, the mixture was concentrated to 2/3 of its volume and poured into ice-water. The pH was adjusted to 3 by the addition of hydrochloric acid and the solid thus obtained was filtered, air dried and triturated with 1-chlorobutane to yield 10.6 g of N-(butylaminocarbonyl)-3-methyl-2-thiophenesulfonamide melting at 144°-146°. It showed absorption peaks by NMR (60 MC) at 2.6 δ (singlet, CH3), 1-1.8 δ (mult., C3H7), 3.42 δ (trip., N-Ch2 - of butyl) and at 7.1 δ and 7.7 δ (2 doublets for CH's of thiophene) consistent for the desired structure.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04398939 |
| 出典データセット | uspto-grants-1983_08 |
| ORD ID | ord-841ce0dc23754fa7b349f1ab76292de2 |
| 出典メモ | uspto-grants-1983_08 |