1-Bromo-3-methylbutane → [1-(3-Methyl-butyl)-2-oxo-1,2,3,4-tetrahydro-quinolin-3-yl]-acetic acid methyl ester

HRID 2105545노트

반응식

HRID 2105545 반응식
[CH3:1][O:2][C:3](=[O:16])[CH2:4][CH:5]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[NH:7][C:6]1=[O:15].Br[CH2:18][CH2:19][CH:20]([CH3:22])[CH3:21]>>[CH3:1][O:2][C:3](=[O:16])[CH2:4][CH:5]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[N:7]([CH2:18][CH2:19][CH:20]([CH3:22])[CH3:21])[C:6]1=[O:15]

참가 물질

3

실험 절차

Following a similar N-alkylation procedure described in example 9, the (2-oxo-1,2,3,4-tetrahydro-quinolin-3-yl)-acetic acid methyl ester (0.068 mmol) obtained in the previous step is alkylated with 1-bromo-3-methylbutane to give the crude [1-(3-methyl-butyl)-2-oxo-1,2,3,4-tetrahydro-quinolin-3-yl]-acetic acid methyl ester, which is used in the next step without further purification.

출처 및 근거

ORD 기록
ord-833df7691f224511bae6ad23026ea0ba
출처 데이터셋
uspto-grants-2009_08
특허 번호
US07579363B2

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