Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1514164생성일: 2026년 10월 26일
Ethyl Acetate → N-(cyclohexylmethyl)-2-{3-[4-(2-methoxyphenyl)piperazin-1-yl]butanoyl}hydrazinecarboxamide
https://huagongshe.com/reaction/1514164
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | (Isocyanatomethyl)cyclohexane | HCID 3414518 | — |
| 반응물 | 3-[4-(2-Methoxyphenyl)piperazin-1-yl]butanohydrazide | HCID 59536465 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | N-(cyclohexylmethyl)-2-{3-[4-(2-methoxyphenyl)piperazin-1-yl]butanoyl}hydrazinecarboxamide | HCID 59536457 | — |
반응 단계
To a suspension of 3-[4-(2-methoxyphenyl)piperazin-1-yl]butanohydrazide D12 (0.5 g, 1.71 mmol) in anhydrous toluene (7 mL), cyclohexanemethyl isocyanate (0.25 g, 1.80 mmol) was added dropwise at room temperature, the mixture was heated at 100° C. and stirred for 10 min. The solution was allowed to cool slowly to room temperature, AcOEt (15 mL) was added and the organic phase was washed with water (2×10 mL), dried over MgSO4 and evaporated under reduced pressure to afford 0.909 g N-(cyclohexylmethyl)-2-{3-[4-(2-methoxyphenyl)piperazin-1-yl]butanoyl}hydrazinecarboxamide D13 as an orange oil. The product containing little toluene was used in the next step without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08222254B2 |
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| 출처 데이터셋 | uspto-grants-2012_07 |
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| ORD ID | ord-eb1088f431054907a5c786af232139cd |
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| 출처 메모 | uspto-grants-2012_07 |
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