Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54964생성일: 2026년 10월 25일
Potassium Chloride → 1,2,4,5-Tetrahydro-4-methyl-1-phenyl-3H-2,4-benzodiazepin-3-thione
https://huagongshe.com/reaction/54964
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Chloride | HCID 4873 | — |
| 반응물 | Carbon Disulfide | HCID 6348 | — |
| 반응물 | Potassium Acetate | HCID 517044 | — |
| 반응물 | Carbamodithioic acid | HCID 3001860 | — |
| 반응물 | 2-[(Methylamino)methyl]-alpha-phenylbenzenemethanamine dihydrochloride | HCID 19957059 | — |
| 용매 | Isopropanol | HCID 3776 | — |
| 생성물 | 1,2,4,5-Tetrahydro-4-methyl-1-phenyl-3H-2,4-benzodiazepin-3-thione | HCID 14978307 | 38% |
반응 단계
To a suspension of 15 g (50 mmol) of 2-[(methylamino)methyl]-α-phenylbenzenemethanamine dihydrochoride 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 of potassium chloride, was filtered off. The carbamodithioic acid was suspended in 125 mL of 95% ethanol, and 1.3 mL of 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05624922 |
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| 출처 데이터셋 | uspto-grants-1997_04 |
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| ORD ID | ord-2068da37eed34df5b6bdbddc2bfafcbc |
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| 출처 메모 | uspto-grants-1997_04 |
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