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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Propylphosphonic anhydride | HCID 111923 | — |
| 반응물 | Ethyldiisopropylethylamine | HCID 18997630 | — |
| 반응물 | 3-(ethoxycarbonyl)-1-methyl-1H-pyrazole-4-carboxylic acid | HCID 45600696 | — |
| 반응물 | 2-Phenylimidazo[1,2-A]pyrimidin-7-amine | HCID 50878390 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 1-Methyl-4-(2-phenyl-imidazo[1,2-a]pyrimidin-7-ylcarbamoyl)-1H-pyrazole-3-carboxylic acid ethyl ester | HCID 67392329 | 29.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08410117B2 |
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| 출처 데이터셋 | uspto-grants-2013_04 |
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| ORD ID | ord-a10c765232c14f5096b2de306d39ef4b |
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| 출처 메모 | uspto-grants-2013_04 |
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