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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 630657생성일: 2026년 10월 25일

(2S)-2-amino-5-(((tert-butoxy)carbonyl)amino)pentanoic acid → HCID 89545074, 화합물

https://huagongshe.com/reaction/630657

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참여 물질

역할이름HCID투입량
반응물(2S)-2-amino-5-(((tert-butoxy)carbonyl)amino)pentanoic acidHCID 6993436—
반응물HCID 117612078HCID 117612078—
용매DichloromethaneHCID 6344—
생성물HCID 89545074HCID 89545074—

반응 조건

온도75 °C

반응 단계

3.00 g (6.16 mmol) of the compound from example 1A was dissolved in 60 ml dichloromethane. 1.43 g (6.16 mmol) N5-(tert-Butoxycarbonyl)-L-ornithine was added. The reaction mixture was split into 3 portions. The portions were heated for 30 min in a sealed tube at 75° C. in a microwave synthesizer. The combined reaction mixture was extracted with approx. 500 ml saturated ammonium chloride solution. The aqueous phase was twice back extracted with approx. 30 ml dichloromethane each. The combined organic phases were extracted with approx. 50 ml brine and dried over sodium sulfate. The solvent was removed under reduced pressure. The raw product was dissolved in dichloromethane and chromatographed over approx. 500 ml silica gel. Solvents used were dichloromethane, dichloromethane/methanol 20/1 to dichloromethane/methanol 1/1. The product-containing fractions were combined and concentrated to dryness under reduced pressure. This gave 2.29 g (3.50 mmol, 57% of theory, 89% purity) of the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09315543B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-825d5db757324a8d9ac38bfcd3757466
출처 메모uspto-grants-2016_04