참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Isobutylene oxide | HCID 11208 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | HCID 178526745 | HCID 178526745 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-methyl-1-(3-nitro-1H-pyrazol-1-yl)propan-2-ol | HCID 54594440 | 54% |
반응 단계
A solution of 3-nitro-1H-pyrazole (prepared in Example 3, 200 mg, 1.77 mmol) in N,N-dimethylformamide (5 mL) was treated with solid potassium carbonate (352 mg, 2.55 mmol) and 2,2-dimethyl-oxirane (314 mL, 3.54 mmol) and placed in a sealed tube and heated to 100° C. for 1 h in an oil bath. After this time the reaction was cooled to 25° C. and diluted with water (10 mL) and extracted with ethyl acetate (3×10 mL). The organic layers were then combined and dried over sodium sulfate, filtered and concentrated in vacuo. Purification by AnaLogix Intelliflash system (12 g column, 50% ethyl acetate/hexanes to 60% ethyl acetate/hexanes) afforded 2-methyl-1-(3-nitro-pyrazol-1-yl)-propan-2-ol (175 mg, 54%) as a clear colorless oil: ES-HRMS m/e calcd for C7H11N3O3 (M+H)+ 186.0873, observed 186.0873; 1H NMR (300 MHz, CDCl3) δ ppm 1.25 (s, 6H, 2×CH3), 2.11 (br. s., 1H, OH), 4.18 (s, 2H, NCH2), 6.92 (d, J=2.4 Hz, 1H, Ar), 7.60 (d, J=2.4 Hz, 1H, Ar).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07935699B2 |
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| 출처 데이터셋 | uspto-grants-2011_05 |
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| ORD ID | ord-c455a7a8fad74520b5baa736268fa4f8 |
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| 출처 메모 | uspto-grants-2011_05 |
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