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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1958333생성일: 2026년 10월 27일

Propylphosphonic anhydride → 1-Methyl-4-(2-phenyl-imidazo[1,2-a]pyrimidin-7-ylcarbamoyl)-1H-pyrazole-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1958333

반응식

참여 물질

역할이름HCID투입량
반응물Propylphosphonic anhydrideHCID 111923—
반응물EthyldiisopropylethylamineHCID 18997630—
반응물3-(ethoxycarbonyl)-1-methyl-1H-pyrazole-4-carboxylic acidHCID 45600696—
반응물2-Phenylimidazo[1,2-A]pyrimidin-7-amineHCID 50878390—
용매Ethyl AcetateHCID 8857—
생성물1-Methyl-4-(2-phenyl-imidazo[1,2-a]pyrimidin-7-ylcarbamoyl)-1H-pyrazole-3-carboxylic acid ethyl esterHCID 6739232929.7%

반응 조건

온도0 °C

반응 단계

At 0° C., propylphosphonic acid anhydride (1-propanephosphonic acid cyclic anhydride, 50% in ethyl acetate, 7.4 ml, 2.5 eq.) was added slowly to a solution of 2-phenylimidazo[1,2-a]pyrimidin-7-amine (example 1, step 1, 1.27 g, 6 mmol), 1-methyl-1H-pyrazole-3,4-dicarboxylic acid 3-ethyl ester (1.00 g, 5 mmol), and ethyldiisopropylethylamine (2.0 ml, 15 mmol) in ethyl acetate (20 ml). The mixture was stirred for 30 min at 0° C., and subsequently at RT for 48 h. The mixture was taken up in ethyl acetate, and washed with water. The combined water layers were adjusted to pH=9 (NaOH), and extracted with dichloromethane. All organic layers were combined, dried (Na2SO4), and evaporated. The title compound (580 mg, 29%) was obtained from the residue by column chromatography (silica gel, heptane:ethyl acetate=100:0-80:20). (1-Methyl-1H-pyrazole-3,4-dicarboxylic acid 3-ethyl ester was obtained by the method of Pérez et al., Spanish patent appl. ES 493459.)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08410117B2
출처 데이터셋uspto-grants-2013_04
ORD IDord-a10c765232c14f5096b2de306d39ef4b
출처 메모uspto-grants-2013_04