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5,5-Dimethyl-2,4-imidazolidinedithione → 2,4-bis(3-dimethylaminobenzylthio)-5,5-dimethyl-5H-imidazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 5,5-Dimethyl-2,4-imidazolidinedithione | HCID 3002142 | — |
| 反応物 | Sodium Methoxide | HCID 10942334 | — |
| 反応物 | 3-(chloromethyl)-N,N-dimethylaniline hydrochloride | HCID 18934895 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 2,4-bis(3-dimethylaminobenzylthio)-5,5-dimethyl-5H-imidazole | HCID 18934902 | — |
反応手順
Initially, 2.94 g of 3-dimethylaminobenzylchloride hydrochloride was added to a mixture of 1.6 g of 5,5-dimethyl-2,4-dithiohydantoin and 1.3 g of sodium methoxide in 50 mL of methanol (MeOH). The reaction mixture was stirred at the room temperature for one hour, and concentrated in vacuo. The residue was treated following the procedure used in Example 56, and chromatographed on a column of silica gel (CHCl3). From the earlier fractions, 2,4-bis(3-dimethylaminobenzylthio)-5,5-dimethyl-5H-imidazole was isolated, in the form of a syrup. The yield of this compound was 0.31 g with a yield ratio of 7.4%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05733922 |
| 出典データセット | uspto-grants-1998_03 |
| ORD ID | ord-483dd6c046dd4bfda158d9c42f0f2afc |
| 出典メモ | uspto-grants-1998_03 |