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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

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물2-(Pyridin-4-yl)-1,3-thiazole-4-carboxylic acidHCID 716091—
반응물(R)-2-amino-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydronaphthaleneHCID 53960413—
용매DimethylformamideHCID 6228—
생성물(R)-N-[8-(4-Methylpiperazin-1-yl)-1,2,3,4-tetrahydro-2-naphthyl]-2-(4-pyridyl)thiazole-4-carboxamideHCID 5454804261.9%

반응 조건

온도75 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06410530B1
출처 데이터셋uspto-grants-2002_06
ORD IDord-a3e861d8dcb7486bb53780613e1abaf5
출처 메모uspto-grants-2002_06