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HRID 1769110作成日:2026年10月26日

Potassium Chloride → 1,2,4,5-Tetrahydro-4-methyl-1-phenyl-3H-2,4-benzodiazepin-3-thione

https://huagongshe.com/reaction/1769110

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium ChlorideHCID 4873—
反応物Carbon DisulfideHCID 6348—
反応物Potassium AcetateHCID 517044—
反応物Carbamodithioic acidHCID 3001860—
反応物2-[(Methylamino)methyl]-alpha-phenylbenzenemethanamine dihydrochlorideHCID 19957059—
溶媒IsopropanolHCID 3776—
生成物1,2,4,5-Tetrahydro-4-methyl-1-phenyl-3H-2,4-benzodiazepin-3-thioneHCID 1497830738%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05380721
出典データセットuspto-grants-1995_01
ORD IDord-f0ac08a8be49426cafff99098869b47e
出典メモuspto-grants-1995_01