참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Toluene | HCID 1140 | — |
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Phosphorus oxychloride | HCID 24813 | — |
| 반응물 | HCID 178446845 | HCID 178446845 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 2-Butyl-5-chloro-1H-imidazole-4-carbaldehyde | HCID 55176 | — |
반응 단계
Phosphorus oxychloride (43.80 g, mmol) was added to a suspension of (pentanimidoylamino)acetic acid (15.82 g, 100 mmol) in toluene (75 ml) in the course of 5 minutes. The mixture was heated to 80° C. and then admixed with N,N-dimethylformamide (20.57 g, 280 mmol) in the course of 7 minutes. The temperature rose in the course of this to 96° C. After stirring for 2 hours at 100° C., the mixture was cooled to 30° C. The reaction mixture was then poured with stirring into 80 ml of water in such a manner that the temperature could always be kept below 30° C. After addition of ethyl acetate (80 ml) and Celite (5 g), the pH of the mixture was adjusted to 1.2 with 30 percent strength sodium hydroxide solution. The mixture was filtered, then phase separation took place at 30° C. The organic phase was washed twice with water and then concentrated to dryness. The title product was obtained in a yield of 13.39 g (HPLC purity 81.4 percent), 50 percent based on (pentanimidoylamino)acetic acid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05696272 |
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| 출처 데이터셋 | uspto-grants-1997_12 |
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| ORD ID | ord-6c5bfe4fab714dd4b330a309566fe50d |
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| 출처 메모 | uspto-grants-1997_12 |
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