참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Azetidine | HCID 10422 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Propylphosphonic anhydride | HCID 111923 | — |
| 반응물 | 1-Methyl-4-nitro-1H-pyrazole-5-carboxylic acid | HCID 592623 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | Azetidin-1-yl(2-methyl-4-nitro-2H-pyrazol-3-yl)methanone | HCID 70096944 | 73.1% |
반응 단계
To a suspension of 2-methyl-4-nitro-2H-pyrazole-3-carboxylic acid (300 mg, 1.75 mmol), azetidine (354 μl, 5.25 mmol) and diisopropylethylamine (920 μl, 5.26 mmol) in ethyl acetate (7.5 ml) was added 1-propanephosphonic acid cyclic anhydride (3.68 ml, 6.13 mmol; 50% in ethyl acetate) at 0° C. The ice bath was removed and stirring at r.t. was continued for 40 h. The reaction mixture was poured into ethyl acetate (100 ml) and extracted with sodium bicarbonate (saturated aqueous solution) water and brine. The aqueous layer was back-extracted with ethyl acetate, the combined organic phases were dried, evaporated, and the product was purified by silica gel chromatography using an amine phase and a heptane/ethyl acetate gradient to yield a white solid (269 mg, 73%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08623866B2 |
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| 출처 데이터셋 | uspto-grants-2014_01 |
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| ORD ID | ord-c2cf414c53c4417d83812f8997482572 |
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| 출처 메모 | uspto-grants-2014_01 |
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