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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 231405생성일: 2026년 10월 26일

2-Amino-4,6-dimethoxypyrimidine → 4-(Cyclopropylcarbonyl)-N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-1-methyl-1H-pyrazole-5-sulfonamide

https://huagongshe.com/reaction/231405

반응식

참여 물질

역할이름HCID투입량
반응물2-Amino-4,6-dimethoxypyrimidineHCID 118946—
반응물4-Cyclopropylcarbonyl-1-methyl-5-pyrazolesulfonamideHCID 14230998—
반응물PhenylcarbamateHCID 21896570—
반응물HCID 22171225HCID 22171225—
용매AcetonitrileHCID 6342—
생성물4-(Cyclopropylcarbonyl)-N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-1-methyl-1H-pyrazole-5-sulfonamideHCID 14230999—

반응 단계

To a stirring mixture of the sulfonamide from Example 2 (175 mg, 0.76 mmol) and the phenylcarbamate of 4,6-dimethoxy-2-aminopyrimidine (210 mg, 0.76 mmol) in 3 ml of acetonitrile was added diazobicycloundecane (116 mg, 0.76 mmol). The solution was stirred for approximately 10 minutes. Acidification of the reaction mixture and filtration of the resulting solids afforded 300 mg of the desired compound m.p. 189°-192° C. NMR (200 MHz, CDCl3) 1.0 (m, 2H), 1.1 (m, 2H), 2.4 (m, 1H), 4.0 (s, 6H), 4.35 (s, 1H), 5.80 (s, 1H), 7.4 (br. s, 1H), 8.05 (s, 1H), 12.9 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04846878
출처 데이터셋uspto-grants-1989_07
ORD IDord-5b8f307d02064ce6995a15186cec2310
출처 메모uspto-grants-1989_07