참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methyl chloroformate | HCID 6586 | — |
| 반응물 | 4-Methylmorpholine | HCID 7972 | — |
| 반응물 | 2-Methoxycyclohexan-1-amine | HCID 22250879 | — |
| 반응물 | HCID 178482013 | HCID 178482013 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-(4-methoxycyclohexyl)-4-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-butyramide | HCID 53790851 | 43% |
반응 단계
To methylene chloride (50 ml) are added 4-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-butyric acid (45 mmole) and N-methylmorpholine (50 mmole). To the mixture is added dropwise with stirring methyl chloroformate (50 mmole) with keeping the inner temperature at 10°-20° C. by ice-cooling, and thereafter, the mixture is stirred at room temperature for 30 minutes. To the mixture is added 2-methoxycyclohexylamine (54 mmole), and the mixture is stirred at the same temperature for 4 hours. After the reaction, water is added to the reaction mixture. The organic layer is separated and washed with dilute aqueous sodium hydroxide solution, diluted hydrochloric acid and water in order, and dried over sodium sulfate. Inorganic materials are filtered off, and the mother liquor is concentrated. The resulting residue is subjected to column chromatography (Wakogel C-200, eluting solvent, benzene:chloroform=4:1, V/V) to isolate N-(4-methoxycyclohexyl)-4-(1-methyl-1,2,3,4-tetrazol-5-yl)thio-butyramide (yield: 43%), colorless liquid, nD11 =1.5263.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04766120 |
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| 출처 데이터셋 | uspto-grants-1988_08 |
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| ORD ID | ord-f211f03e53b04a2a9cb7041bab37de39 |
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| 출처 메모 | uspto-grants-1988_08 |
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