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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 978028생성일: 2026년 10월 24일

Isobutyl chloroformate → N-[4-(N,N-dimethylamino)cyclohexyl]-4-(1-methyl-1,2,3,4-tetrazol-5-yl)thiobutyramide

https://huagongshe.com/ko/reaction/978028

반응식

참여 물질

역할이름HCID투입량
반응물Isobutyl chloroformateHCID 62365—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물N,N-Dimethyl-1,4-cyclohexanediamineHCID 345823—
반응물HCID 178482013HCID 178482013—
용매TetrahydrofuranHCID 8028—
생성물N-[4-(N,N-dimethylamino)cyclohexyl]-4-(1-methyl-1,2,3,4-tetrazol-5-yl)thiobutyramideHCID 2129529947%

반응 단계

4-(1-Methyl-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 4-(N,N-dimethylamino)cyclohexylamine (54 mmole), and the mixture is further stirred at room temperature for 2 hours. After distilling off the solvent under reduced pressure, the resulting 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. Chloroform is distilled off, and the resulting residue is subjected to silica gel column chromatography (Wakogel C-200, eluting solvent, benzene:chloroform=4:1, V/V) to isolate N-[4-(N,N-dimethylamino)-cyclohexyl]-4-(1-methyl-1,2,3,4-tetrazol-5-yl)thiobutyramide (yield: 47%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04663323
출처 데이터셋uspto-grants-1987_05
ORD IDord-ac78e6b749174eb5b0d8d4b817a1e21c
출처 메모uspto-grants-1987_05