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2-[6-(Methylamino)-2-pyridyl]ethan-1-ol → 3-[5-[2-(6-Methylamino-pyridin-2-yl)-ethoxy]-indol-1-yl}-hexanoic acid ethyl ester

HRID 1295176
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인쇄 미리보기

반응식

HRID 1295176 반응식
[CH3:1][NH:2][C:3]1[N:8]=[C:7]([CH2:9][CH2:10][OH:11])[CH:6]=[CH:5][CH:4]=1.[CH2:12]([O:14][C:15](=[O:31])[CH2:16][CH:17]([N:21]1[C:29]2[C:24](=[CH:25][C:26](O)=[CH:27][CH:28]=2)[CH:23]=[CH:22]1)[CH2:18][CH2:19][CH3:20])[CH3:13]>>[CH2:12]([O:14][C:15](=[O:31])[CH2:16][CH:17]([N:21]1[C:29]2[C:24](=[CH:25][C:26]([O:11][CH2:10][CH2:9][C:7]3[CH:6]=[CH:5][CH:4]=[C:3]([NH:2][CH3:1])[N:8]=3)=[CH:27][CH:28]=2)[CH:23]=[CH:22]1)[CH2:18][CH2:19][CH3:20])[CH3:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 105348582-[6-(Methylamino)-2-pyridyl]ethan-1-olHCID 674263943-(5-Hydroxy-indol-1-yl)-hexanoic acid ethyl ester

생성물 1

HCID 674277183-[5-[2-(6-Methylamino-pyridin-2-yl)-ethoxy]-indol-1-yl}-hexanoic acid ethyl ester수율 25%

실험 절차

The title compound was synthesized from 2-(6-methylamino-pyridin-2-yl)-ethanol and 3-(5-hydroxy-indol-1-yl)-hexanoic acid ethyl ester using the procedure described in Example 14, step (c), in 25% yield. The crude product was used in the next step without further purification.

후처리

  1. customThe crude product was used in the next step without further purification

출처 및 근거

ORD 기록
ord-e931377ee4a24c7baca32a9b944e7f94
출처 데이터셋
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07241789B2

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