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Benzyl Isothiocyanate → N-Benzyl-N'-(3-chloro-5-trifluoromethyl-2-pyridyl)methylthiourea
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzyl Isothiocyanate | HCID 2346 | — |
| 反応物 | 1-[3-Chloro-5-(trifluoromethyl)pyridin-2-yl]methanamine--hydrogen chloride (1/1) | HCID 11499744 | — |
| 触媒 | Triethylamine | HCID 8471 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | N-Benzyl-N'-(3-chloro-5-trifluoromethyl-2-pyridyl)methylthiourea | HCID 22637232 | — |
反応手順
To a mixture of (3-chloro-5-trifluoromethyl-2-pyridyl)methylamine hydrochloride (0.12 g) and benzylisothiocyanate (0.11 g) in dry tetrahydrofuran (10 ml) was added triethylamine (10 drops) and the mixture stirred at room temperature for 12 hours. The solvent was evaporated and ethyl acetate added. The mixture was washed with 2M hydrochloric acid and then with saturated sodium bicarbonate solution. The organic layer was separated and the solvent removed to give the title product. 1H N.M.R. δ(ppm) 4.7 (2H, broad s), 4.95 (2H, d), 6.9 (1H, broad s), 7.3-7.55 (6H, m), 7.95 (1H, s) and 8.58 (1H, s).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06821992B1 |
| 出典データセット | uspto-grants-2004_11 |
| ORD ID | ord-28e0e1d6a64047fa93a0ce93b34299c0 |
| 出典メモ | uspto-grants-2004_11 |