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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1769110생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1769110

반응식

참여 물질

역할이름HCID투입량
반응물Potassium ChlorideHCID 4873—
반응물Carbon DisulfideHCID 6348—
반응물Potassium AcetateHCID 517044—
반응물Carbamodithioic acidHCID 3001860—
반응물2-[(Methylamino)methyl]-alpha-phenylbenzenemethanamine dihydrochlorideHCID 19957059—
용매IsopropanolHCID 3776—
생성물1,2,4,5-Tetrahydro-4-methyl-1-phenyl-3H-2,4-benzodiazepin-3-thioneHCID 1497830738%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05380721
출처 데이터셋uspto-grants-1995_01
ORD IDord-f0ac08a8be49426cafff99098869b47e
출처 메모uspto-grants-1995_01