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2-Amino-4,5,6,7-tetrahydrobenzothiazole → N-[2-(1-cyclohexenyl)ethyl]-N'-[4,5,6,7-tetrahydrobenzothiazolyl]thiourea
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Amino-4,5,6,7-tetrahydrobenzothiazole | HCID 18046 | — |
| 反応物 | 1-(2-Isothiocyanatoethyl)cyclohex-1-ene | HCID 2735881 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | N-[2-(1-cyclohexenyl)ethyl]-N'-[4,5,6,7-tetrahydrobenzothiazolyl]thiourea | HCID 19703901 | 13.3% |
反応手順
A solution of 2-(1-cyclohexenyl)ethyl isothiocyanate (1.67 g, 10 mmol) and 2-amino-4,5,6,7-tetrahydrobenzothiazole (1.54 g, 10 mmol) in N,N-dimethylformamide (100 mL) was heated at 100° C. for 120 h. The reaction was cooled to room temperature, the solvent removed under reduced pressure, the residue taken up in ethyl acetate and washed with 1N HCl. The organic layer was concentrated and the residue recrystallized from ethyl acetate-hexanes to provide 426 mg (13%) of the titled product:
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05593993 |
| 出典データセット | uspto-grants-1997_01 |
| ORD ID | ord-d5c227c25b4b45b1b6cd865fee535c41 |
| 出典メモ | uspto-grants-1997_01 |