Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132906생성일: 2026년 10월 25일
N-(2-Cyanophenyl)piperazine → 3-(4-Chloro-3-methyl-phenyl)-1-{3-[4-(2-cyano-phenyl)-piperazin-1-yl]-2-hydroxy-propyl}-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridine-5-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/132906
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | N-(2-Cyanophenyl)piperazine | HCID 2735875 | — |
| 반응물 | 3-(4-Chloro-3-methyl-phenyl)-1-oxiranylmethyl-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridine-5-carboxylic acid tert-butyl ester | HCID 86584817 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Triethylamine | HCID 8471 | — |
| 생성물 | 3-(4-Chloro-3-methyl-phenyl)-1-{3-[4-(2-cyano-phenyl)-piperazin-1-yl]-2-hydroxy-propyl}-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridine-5-carboxylic acid tert-butyl ester | HCID 68462199 | 83.4% |
반응 단계
3-(4-Chloro-3-methyl-phenyl)-1-oxiranylmethyl-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridine-5-carboxylic acid tert-butyl ester (5.33 g, 13.2 mmol) and 1-(2-cyanophenyl)-piperazine (2.97 g, 15.86 mmol) were partially dissolved in EtOH (50 mL) and triethylamine (2 mL). The reaction mixture was heated to 80° C. for 18 h. The mixture was concentrated and purified by column chromatography (silica, 20% acetone/CH2Cl2) to give 3-(4-chloro-3-methyl-phenyl)-1-{3-[4-(2-cyano-phenyl)-piperazin-1-yl]-2-hydroxy-propyl}-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridine-5-carboxylic acid tert-butyl ester (6.51 g, 83%) as a yellow solid. TLC (silica, 20% acetone/CH2Cl2): Rf=0.35. MS (electrospray): m/z 591.3 (591.3, calculated for C32H39CIN6O3, [M+H]+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07388011B2 |
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| 출처 데이터셋 | uspto-grants-2008_06 |
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| ORD ID | ord-4a464791635e4ba3afb183eebde49055 |
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| 출처 메모 | uspto-grants-2008_06 |
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