참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Acetonitrile | HCID 6342 | — |
| 반응물 | Trimethyl orthoformate | HCID 9005 | — |
| 반응물 | L-2,4-Diaminobutyric acid | HCID 134490 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | CID 137208342 | HCID 137208342 | — |
반응 단계
60 ml of trimethyl orthoformate are dissolved in 400 ml of methanol, and reacted with 30 g of L-diaminobutyric acid×2 HCl at 55° C. with constant stirring. After a reaction time of 2 hours, the solvent is evaporated under reduced pressure, the crude product which remains is dissolved in 50 ml of demineralized water, and the solution is neutralized using NaOH. The compound is subsequently purified on an ion retardation column type BIORAD® AG11A8 (Bio-Rad Laboratories GmbH, Munich, Germany) using demineralized water as the eluent, and the product is dried and recrystallized from methanol. The compound obtained can be identified by means of high-pressure liquid chromatography (HPLC); (for example E. Merck, Darmstadt, Germany, LiChroCART® 125-NH2 5μ, eluent: 80% acetonitrile), and is characterized by the following 13C-NMR data: 176.8, 161.2, 53.8, 37.9, 22.0, 18.7 ppm (relative to TMS); (Galinski E. A., Pfeiffer H. P., Truper H. G. (1985) Eur. J. Biochem. 149, 135-139).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06060071 |
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| 출처 데이터셋 | uspto-grants-2000_05 |
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| ORD ID | ord-baef40fea698453b9508ff2d92d91117 |
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| 출처 메모 | uspto-grants-2000_05 |
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