참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-Chloromethylnaphthalene | HCID 6845 | — |
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | (E)-N-methyl-6,6-dimethyl-2-hepten-4-ynylamine hydrochloride | HCID 19917487 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 생성물 | Terbinafine Hydrochloride | HCID 5282481 | 90% |
반응 단계
To a solution of 1.77 g (10 mmol) of 1-chloromethylnaphthalene in 10 ml of dimethyl sulfoxide were added 1.88 g (10 mmol) of (E)-N-(6,6-dimethyl-2-hepten-4-ynyl)methylamine hydrochloride and 1.66 g (12 mmol) of potassium carbonate under ice cooling. The mixture was stirred for 16 hours at room temperature, poured into 200 ml of ethyl acetate, washed with 100 ml ×2 of water, a mixture of 80 ml of water and 10 ml of 2N hydrochloric acid, and 50 ml of saturated sodium chloride aqueous solution respectively, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to crystallize. The crystals were suspended in 10 ml of ethyl acetate, cooled, filtered and dried under reduced pressure to obtain 2.95 g (yield: 90%) of the above identified compound as off-white crystalline powder.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05296612 |
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| 출처 데이터셋 | uspto-grants-1994_03 |
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| ORD ID | ord-2e2fa72e292e4c488be5080fd157f097 |
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| 출처 메모 | uspto-grants-1994_03 |
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