참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ammonium Bicarbonate | HCID 14013 | — |
| 반응물 | ethyl (2RS)-2-acetylamino-3-(3-cyanophenyl)propanoate | HCID 85797672 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | ethyl (2R)-2-acetylamino-3-(3-cyanophenyl)propanoate | HCID 86584426 | 47.4% |
반응 단계
The process is performed as in Example 2, starting with 11.39 g of ethyl (2RS)-2-acetylamino-3-(3-cyanophenyl)propanoate, 17.39 g of ammonium hydrogen carbonate and 0.1 g of α-chymotrypsin in 200 cm3 of water and 70 cm3 of acetonitrile. After stirring for 24 hours at a temperature in the region of 20° C. and an identical work-up, 5.40 g of ethyl (2R)-2-acetylamino-3-(3-cyanophenyl)propanoate are obtained in the form of a beige-colored solid. (Rf=0.76 in a 40/10/20 by volume mixture of n-butanol/acetic acid/water, on a Merck 60F254R silica plate).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06699895B2 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
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| ORD ID | ord-e4dd21c7908148a8aeb2c86ba6a87e89 |
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| 출처 메모 | uspto-grants-2004_03 |
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