Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2187418생성일: 2026년 10월 26일
Carbon Dioxide → (R)-N-[8-(4-Methylpiperazin-1-yl)-1,2,3,4-tetrahydro-2-naphthyl]-2-(4-pyridyl)thiazole-4-carboxamide
https://huagongshe.com/reaction/2187418
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Carbon Dioxide | HCID 280 | — |
| 반응물 | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| 반응물 | 2-(Pyridin-4-yl)-1,3-thiazole-4-carboxylic acid | HCID 716091 | — |
| 반응물 | (R)-2-amino-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydronaphthalene | HCID 53960413 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (R)-N-[8-(4-Methylpiperazin-1-yl)-1,2,3,4-tetrahydro-2-naphthyl]-2-(4-pyridyl)thiazole-4-carboxamide | HCID 54548042 | 61.9% |
반응 단계
To a solution of 4-carboxy-2-(4-pyridyl)thiazole (89 mg, 0.43 mmol) in anhydrous N,N-dimethylformamide (25 mL) was added 1,1′-carbonyldiimidazole (73 mg, 0.45 mmol) and the reaction was heated at 75° C. When the carbon dioxide evolution had ceased (after 30 min), the reaction was cooled to room temperature and a solution of (R)-2-amino-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydronaphthalene (100 mg, 0.41 mmol) in anhydrous N,N-dimethylformamide (5 mL) was added. The reaction was allowed to stir at ambient temperature for 17 h and the solvent was evaporated in vacuo. Purification on a silica gel column using chloroform/ethanol saturated with NH3 (100:3) as the eluent gave 110 mg (61% yield) of the title compound as white crystals: mp 187-188° C.; [α]21D '82° (c 1.0, chloroform); EIMS (70 eV) m/z (relative intensity) 433 (2, M+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06410530B1 |
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| 출처 데이터셋 | uspto-grants-2002_06 |
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| ORD ID | ord-a3e861d8dcb7486bb53780613e1abaf5 |
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| 출처 메모 | uspto-grants-2002_06 |
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