참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2,4-Dimethoxybenzonitrile | HCID 77750 | — |
| 반응물 | 4,5-Diaminopyrimidine | HCID 83703 | — |
| 반응물 | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| 용매 | Benzene | HCID 241 | — |
| 생성물 | 1H-Purine, 8-(2,4-dimethoxyphenyl)- | HCID 3059912 | — |
반응 단계
A mixture of 2 g of 4,5-diamino-pyrimidine, 4 g of 2,4-dimethoxy-benzonitrile, 6 g of p-toluene sulfonic acid hydrate, and 40 ml of benzene was heated, whereby the benzene was distilled off. The residue was heated for 30 minutes at 120° C. After cooling the residue was triturated with 2 N ammonia and extracted with ethyl acetate. The ethyl acetate phase was extracted with 2 N hydrochloric acid, the aqueous phase was neutralized and again extracted with ethyl acetate, and subsequently the organic phase was extracted with 2 N sodium hydroxide solution. When the aqueous phase was neutralized, the product was precipitated and recrystallized from water.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04299834 |
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| 출처 데이터셋 | uspto-grants-1981_11 |
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| ORD ID | ord-63f0d60977ab4bd0987398e8ee4f424a |
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| 출처 메모 | uspto-grants-1981_11 |
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