(2S)-2-(((tert-butoxy)carbonyl)amino)pentanoic acid → methyl N-(tert-butoxycarbonyl)-L-norvalyl-L-threoninate

HRID 869730

반응식

HRID 869730 반응식
[C:1]([O:5][C:6]([NH:8][C@H:9]([C:13]([OH:15])=O)[CH2:10][CH2:11][CH3:12])=[O:7])([CH3:4])([CH3:3])[CH3:2].Cl.[CH2:17]([O:19][C:20](=[O:26])[C@H:21]([C@@H:23]([CH3:25])[OH:24])[NH2:22])C>>[C:1]([O:5][C:6]([NH:8][C@H:9]([C:13]([NH:22][C@H:21]([C:20]([O:19][CH3:17])=[O:26])[C@@H:23]([CH3:25])[OH:24])=[O:15])[CH2:10][CH2:11][CH3:12])=[O:7])([CH3:2])([CH3:3])[CH3:4]

참가 물질

3

반응물 2

HCID 2733748(2S)-2-(((tert-butoxy)carbonyl)amino)pentanoic acidHCID 2763096Ethyl L-threoninate hydrochloride

생성물 1

HCID 86674524methyl N-(tert-butoxycarbonyl)-L-norvalyl-L-threoninate

실험 절차

The preparation was performed in a similar manner as Example 1.001 (d) Method B from N-(tert-butoxycarbonyl)-L-norvaline (13.0 g, 59.8 mmol) and L-threonine ethyl ester hydrochloride (9.23 g, 54.4 mmol) to give methyl N-(tert-butoxycarbonyl)-L-norvalyl-L-threoninate. MS (APCI): m/z 333 (M+H).

출처 및 근거

ORD 기록
ord-d0aaed4f417b4af3917ef0ff3b95f332
출처 데이터셋
uspto-grants-2015_03
특허 번호
US08969376B2

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