참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acrylonitrile | HCID 7855 | — |
| 반응물 | 1,4-Dioxane | HCID 31275 | — |
| 반응물 | 2-Nitropyridin-3-amine | HCID 83281 | — |
| 반응물 | 3-Amino-4-nitropyridine | HCID 586943 | — |
| 생성물 | Benzyltriethylammonium hydroxide | HCID 74601 | — |
반응 단계
An aminonitropyridine derivative II, such as 3-amino4-nitropyridine, may be treated with a mixture of acrylonitrile and a suitable base such as Triton B (N-benzyltriethylammonium hydroxide) in an appropriate solvent such as dioxane at room temperature for 1-4 days to give the illustrated nitrile derivative III. Treatment of derivative III with a suitable reduction catalyst such as Pd/C in an appropriate solvent such as ethyl acetate under hydrogen atmosphere of about 50-60 psig for about 3-12 h gives the amino derivative IV. This derivative may be heated with ethyl ethoxycarbonylacetimidate hydrochloride in a suitable solvent such as EtOH for about 4-24 h to give the the ester V. Treatment of derivative V with an anhydrous acid such as HCl(g) in an appropriate solvent such as EtOH at reflux for 4-24 h gives the diester VI. This diester may be treated with a suitable base such as sodium ethoxide in an appropriate solvent such as EtOH for about 12-24 h at room temperature followed by treatment with ethanolic HCl to give the derivative
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05968946 |
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| 출처 데이터셋 | uspto-grants-1999_10 |
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| ORD ID | ord-67fbae588a7346c59b4d397f6ee914c0 |
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| 출처 메모 | uspto-grants-1999_10 |
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