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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1433048생성일: 2026년 10월 26일

Diisopropylethylamine → 2-[2-Benzyloxycarbonylamino-propylamino]-pentanoic acid methyl ester

https://huagongshe.com/reaction/1433048

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Benzyl 1-methyl-2-oxoethylcarbamateHCID 563116—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물methyl (2S)-2-aminopentanoate hydrochlorideHCID 14118488—
촉매Acetic AcidHCID 176—
촉매ZincchlorideHCID 3007855—
용매MethanolHCID 887—
생성물2-[2-Benzyloxycarbonylamino-propylamino]-pentanoic acid methyl esterHCID 6902799538.6%

반응 단계

To a solution of [1-methyl-2-oxo-ethyl]-carbamic acid benzyl ester (12.3 g, 69 mmol) and norvaline methylester hydrochloride (11.6 g, 69 mmol) in MeOH (300 mL) is added diisopropyl ethyl amine (9.4 g, 73 mmol) and 2 drops of acetic acid. After 10 min., ZnCl2 (9.46 g, 69 mmol) and sodium cyanoborohydride (8.72 g, 14 mmol) is added. The solution is stirred at ambient for 16 h. The solution is then concentrated. The residue is dissolved in EtOAc and 1N KHSO4. The organic layer is washed with 1N KHSO4, H2O, and sat. NaCl. The organic layer is dried over MgSO4, filtered and concentrated. The crude product is purified by column chromatograghy eluting with a gradient of 20% EtOAc/hexane to 40% EtOAc/hexanes. The title compound (8.6 gm, 26.6 mmol) is obtained as a foam. MS (ion spray) m/z 323, (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07612075B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-aa4a4c2600c048e99a1e0176bd434d07
출처 메모uspto-grants-2009_11