참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Butyric Acid | HCID 264 | — |
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Ammonium Hydroxide | HCID 14923 | — |
| 반응물 | 4-Methyl-3,5-dinitropyridin-2-amine | HCID 5086399 | — |
| 촉매 | Nickel | HCID 935 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 7-methyl-2-propyl-6-[(1-oxobutyl)amino]3H-imidazo[4,5-b]pyridine | HCID 19939737 | — |
반응 단계
A mixture of 2-amino-3,5-dinitro-4-methylpyridine (3.1 g, 15.6 mmol), THF (100 mL), methanol (100 mL) and Raney-nickel (6 mL of a 1:1 suspension in H2O) was stirred under H2 (1 atm.) for 6 h. The mixture was quickly filtered into a receiving flask containing 3 mL of conc. aqueous HCl, and the solvent was removed in vacuo at r.t. To the resulting crude 2,3,5-triamino-3-methylpyridine.HCl complex was added butyric acid (4.3 mL, 46.9 mmol) and polyphosphoric acid (100 mL) and this mixture was heated to 85° C. for 10 h. The warmed mixture was poured into stirred ice-H2O (200 mL) and this mixture was cooled and neutralized (to pH 3) by the addition of conc. NH4OH. Extraction with CH2Cl2 (3×50 mL), drying (Na2SO4), and concentration gave the title compound as a solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05412097 |
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| 출처 데이터셋 | uspto-grants-1995_05 |
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| ORD ID | ord-fc41fdc5d05c49e9b0278ac7ee56e708 |
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| 출처 메모 | uspto-grants-1995_05 |
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