Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1011887생성일: 2026년 10월 27일
4-Methylmorpholine → (1-{3-[(E)-2-(4-Chloro-phenyl)-vinyl]-phenyl}-3,5-diethyl-1H-pyrazol-4-yl)-[4-(1-methyl-piperidin-4-ylmethyl)-piperazin-1-yl]-methanone
https://huagongshe.com/reaction/1011887
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 4-Methylmorpholine | HCID 7972 | — |
| 반응물 | 2-Chloro-4,6-dimethoxy-1,3,5-triazine | HCID 18450 | — |
| 반응물 | 1-((1-Methyl-4-piperidinyl)methyl)piperazine | HCID 2736942 | — |
| 반응물 | 1-{3-[(E)-2-(4-Chloro-phenyl)-vinyl]-phenyl}-3,5-diethyl-1H-pyrazole-4-carboxylic acid | HCID 67313975 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | (1-{3-[(E)-2-(4-Chloro-phenyl)-vinyl]-phenyl}-3,5-diethyl-1H-pyrazol-4-yl)-[4-(1-methyl-piperidin-4-ylmethyl)-piperazin-1-yl]-methanone | HCID 57554975 | — |
반응 단계
A solution of 0.40 g (1.10 mmol) of 1-{3-[(E)-2-(4-chloro-phenyl)-vinyl]-phenyl}-3,5-diethyl-1H-pyrazole-4-carboxylic acid (intermediate 1) and 0.18 g (1.1 mmol) of 2-chloro-4,6-dimethoxy-[1,3,5]triazine were dissolved in 10 ml of MeCN. The solution was then cooled down to 0° C. and 0.32 g=0.35 ml (3.2 mmol) of N-methylmorpholine was added drop by drop. After 2 hours stirring at 0° C., a solution of 0.21 g (1.1 mmol) 1-(1-methyl-piperidin-4-ylmethyl)-piperazine in 3 ml of MeCN was added drop by drop. Then, the mixture was warmed up to RT and stirring continued for 20 hours. Subsequently, it was poured into crashed ice and extracted twice with EtOAc; the organic phases were washed with water, dried over magnesium sulfate, filtered and evaporated. The residue was purified by flash column chromatography (CH2Cl2/MeOH 1:0-7.5:2.5) to afford the title compound as colorless solid. MS: 560.2 (MH+, 1 Cl).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07977358B2 |
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| 출처 데이터셋 | uspto-grants-2011_07 |
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| ORD ID | ord-3cd2c10fc5c24237a856c05cb19d8ee3 |
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| 출처 메모 | uspto-grants-2011_07 |
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