참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2,3-Dimethylpyrazine | HCID 22201 | — |
| 반응물 | 2,3-Dihydro-5,6-dimethylpyrazine | HCID 85225 | — |
| 반응물 | Pyridine, 2-methyl-4-nitro-, 1-oxide | HCID 95291 | — |
| 생성물 | 4-Ethyl-2-methylpyridine | HCID 68307 | — |
| 생성물 | 4-Methoxy-2-methylpyridine | HCID 4737758 | — |
| 생성물 | 2-Methyl-4-methoxypyridine-N-oxide | HCID 10701893 | — |
반응 단계
In the examples, certain of the starting materials were prepared in accordance with methods disclosed in the literature. For example, 2,3-dimethylpyrazine was prepared from 2,3-dimethyl-5,6-dihydropyrazine by the method of G. P. Rizzi, J. Org. Chem. 33, 1333 (1968) which itself was prepared by the procedure of T. Ishiguro and M. Matsumura, Yak. Zass. 78, 229 (1958). 4-Ethyl-2-methylpyridine was prepared by the procedure of Kaiser et al., J. Org. Chem. 38, 71 (1973). 4-Methoxy-2-picoline-N-oxide was prepared by reacting 4-nitro-2-picoline-N-oxide with methanolic potassium carbonate solution according to the general procedure of E. Profft et al., Germany (East) 69, 126; 10/5/69; Chem. Abs. 72, 90309w (1970). The crude product was not purified but was reacted directly with phosphorous trichloride in chloroform solution to give the known 4-methoxy-2-picoline starting material, based upon the general method of Herz and Tsai, J. Am. Chem. Soc. 76, 4184 (1954).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04678501 |
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| 출처 데이터셋 | uspto-grants-1987_07 |
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| ORD ID | ord-fac269ef987e4cdea9a50d4deedd9982 |
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| 출처 메모 | uspto-grants-1987_07 |
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