참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N-Ethyl cyclohexylamine | HCID 21609 | — |
| 반응물 | Isobutyl chloroformate | HCID 62365 | — |
| 반응물 | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| 반응물 | HCID 178489576 | HCID 178489576 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | HCID 21295432 | HCID 21295432 | 45% |
반응 단계
4-[1-(2-Methoxycyclohexyl)-1,2,3,4-tetrazol-5-yl]thio-butyric acid (45 mmole) is dissolved in tetrahydrofuran (50 ml), and thereto is added DBU (50 mmole). To the mixture is added dropwise with stirring isobutyl chloroformate (50 mmole) under ice-cooling, and the mixture is stirred at room temperature for 30 minutes. To the mixture is added dropwise N-ethyl-cyclohexylamine (54 mmole), and the mixture is further stirred at room temperature for 2 hours. The solvent is distilled off under reduced pressure, and the residue is extracted with chloroform. The chloroform layer is washed with 5% aqueous hydrochloric acid, an aqueous saturated sodium hydrogen carbonate solution and an aqueous saturated sodium chloride solution and then dried over anhydrous sodium sulfate. After distilling off chloroform, the resulting residue is subjected to column chromatography (Wakogel C-200, eluting solvent, benzene:chloroform=4:1, V/V) to isolate N-ethyl-N-cyclohexyl-4-[1-(2-methoxycyclohexyl)-1,2,3,4-tetrazol-5-yl]thiobutyramide (yield: 45%).
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-27ca7185f6bc44af8d5416a7ea67b743 |
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| 출처 메모 | uspto-grants-1988_08 |
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