Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 582565생성일: 2026년 10월 26일
3,5-Dimethylpyrazole-1-carboxamidine → N-(3-cyanophenyl)-N'-(1-amidinopiperidin-4-yl)cycloheptylurea
https://huagongshe.com/reaction/582565
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 3,5-Dimethylpyrazole-1-carboxamidine | HCID 97525 | — |
| 반응물 | HCID 54268872 | HCID 54268872 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | N-(3-cyanophenyl)-N'-(1-amidinopiperidin-4-yl)cycloheptylurea | HCID 54155874 | 74.7% |
반응 단계
N-(3-Cyanophenyl)-N'-(piperidin-4-yl)cycloheptylurea (0.05 g, 0.126 mmol) was dissolved in pyridine (2 ml) and 3,5-dimethylpyrazole-1-carboxamidine (0.037 g, 0.188 mmol) was added under a nitrogen atmosphere. The reaction was heated to 110° C. for 6 h, then was allowed to cool and was concentrated to give a viscous amber oil. The product was purfied by HPLC on a Vydec® C-18 column eluting with solvent mixture A (acetonitrile:water:TFA 80:20:0.3) and solvent mixture B (water:TFA 99.7:0.3) using a gradient starting with A:B at 3:97 and changing to A:B at 70:30 over 15 min. The product eluted at 13.8 minutes was concentrated to give N-(3-cyanophenyl)-N'-(1-amidinopiperidin-4-yl)cycloheptylurea as an amorphous solid (0.036 g); LRMS (M+H)+ m/z 341.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05925635 |
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| 출처 데이터셋 | uspto-grants-1999_07 |
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| ORD ID | ord-316411f4a0204f9fa3b97b57b853aed9 |
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| 출처 메모 | uspto-grants-1999_07 |
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