関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Chloride | HCID 4873 | — |
| 反応物 | Carbon Disulfide | HCID 6348 | — |
| 反応物 | Potassium Acetate | HCID 517044 | — |
| 反応物 | Carbamodithioic acid | HCID 3001860 | — |
| 反応物 | 2-[(Methylamino)methyl]-alpha-phenylbenzenemethanamine dihydrochloride | HCID 19957059 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 生成物 | 1,2,4,5-Tetrahydro-4-methyl-1-phenyl-3H-2,4-benzodiazepin-3-thione | HCID 14978307 | 38% |
反応手順
To a suspension of 15 g (50 mmol) of 2-[(methylamino)methyl]-α-phenylbenzenemethanamine dihydrochloride in 100 mL of isopropyl alcohol was added 10 g (100 mmol) of potassium acetate followed by 3.3 mL (55 mmol) of carbon disulfide in 35 mL of isopropyl alcohol. The suspension was stirred at room temperature for one and one-half hours and then refluxed for 30 minutes. The reaction was chilled in ice and the internal salt of the carbamodithioic acid, contaminated with two equivalents of potassium chloride, was filtered off. The carbamodithioic acid was suspended in 125 mL of 95% ethanol, and 1.3 mL of 12N hydrochloric acid was added. The suspension was refluxed for three days, cooled, and 15.3 g (114%) of the crude benzodiazepin-3-thione was filtered off. A 6-g portion of the crude product was recrystallized from 2-ethoxy ethanol to yield 2.0 g (38%) of product, mp 208-209.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05380721 |
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| 出典データセット | uspto-grants-1995_01 |
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| ORD ID | ord-f0ac08a8be49426cafff99098869b47e |
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| 出典メモ | uspto-grants-1995_01 |
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