참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | HCID 178511198 | HCID 178511198 | — |
| 촉매 | Rhodium | HCID 23948 | — |
| 용매 | Ammonia methanol | HCID 21705897 | — |
| 생성물 | Carnosine | HCID 439224 | — |
반응 단계
In a 1-litre pressure autoclave, a solution of 10.00 g (45.0 mmol) of (5)-2-(cyanoacetylamino)-3-(1H-imidazol-4-yl)propionic acid (prepared according to Example 3) in a mixture of 157 g of conc. NH3/methanol (m/m=3:2) was added to 0.88 g of Rh/C (0.4 mol % pure Rh, based on reactant used). The autoclave was closed and flushed twice with 40 bar of nitrogen and once with hydrogen. The mixture was heated to 90° C. and the autoclave was pressurized with 40 bar of hydrogen. After 3 h at 90° C., the reaction mixture was cooled to room temperature, the autoclave was depressurized and the catalyst was filtered off by filtration. An in-process analysis (HPLC) showed that the reaction solution (147.2 g) contained 6.38% (m/m) carnosine, corresponding to a selectivity of 92% for complete conversion. The reaction mixture was then concentrated in a rotary evaporator to 41.2 g. 124 g of ethanol were added dropwise at room temperature and the flask was stored in a refrigerator overnight. On the next day, the precipitate was filtered off, washed with ethanol and dried in a drying oven at 40° C./20 mbar. 7.96 g (78%) of a slightly greenish solid with a content (HPLC) of 98% (m/m) were obtained.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07164028B2 |
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| 출처 데이터셋 | uspto-grants-2007_01 |
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| ORD ID | ord-a64551029581496587ffbd89fd23a637 |
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| 출처 메모 | uspto-grants-2007_01 |
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