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Trifluoroacetic acid → methyl (2S)-2-amino-3-(quinolin-6-yl)propanoate

HRID 74816
노트
인쇄 미리보기

반응식

HRID 74816 반응식
[CH3:1][O:2][C:3]1[C@H:4]([CH2:14][C:15]2[CH:16]=[C:17]3[C:22](=[CH:23][CH:24]=2)[N:21]=[CH:20][CH:19]=[CH:18]3)[N:5]=C(OC)[C@@H](C(C)C)N=1.FC(F)(F)C(O)=[O:28]>O.C(#N)C>[NH2:5][C@@H:4]([CH2:14][C:15]1[CH:16]=[C:17]2[C:22](=[CH:23][CH:24]=1)[N:21]=[CH:20][CH:19]=[CH:18]2)[C:3]([O:2][CH3:1])=[O:28]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 6422Trifluoroacetic acidHCID 866857696-{[(2S,5R)-3,6-dimethoxy-5-(propan-2-yl)-2,5-dihydropyrazin-2-yl]methyl}quinoline

생성물 1

HCID 86685770methyl (2S)-2-amino-3-(quinolin-6-yl)propanoate

시약·촉매·용매 2

HCID 962Water용매HCID 6342Acetonitrile용매

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온도
10 °C

실험 절차

To a solution of #211 (7.3 g, 22.5 mmol, 1 eq.) in water (25 mL) and acetonitrile (80 mL) was added trifluoroacetic acid (9 mL) at 0° C. and the solution was stirred at 10° C. overnight. The organic layer was removed in vacuo and the remaining aqueous layer was basified to pH 9 with sodium carbonate, which was directly used for the next step.

후처리

  1. customThe organic layer was removed in vacuo

출처 및 근거

ORD 기록
ord-4a9bf0aebfb24ab29f3d2c36f70c87d7
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08828401B2

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