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3-Pyrrolidin-2-ylmethylpyridine dihydrochloride → 3-[(1-{[5-(4-Methylphenyl)isoxazol-4-yl]carbonyl}pyrrolidin-2-yl)methyl]pyridine

HRID 1446191
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인쇄 미리보기

반응식

HRID 1446191 반응식
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[O:12][N:11]=[CH:10][C:9]=2[C:13]([OH:15])=O)=[CH:4][CH:3]=1.Cl.Cl.[NH:18]1[CH2:22][CH2:21][CH2:20][CH:19]1[CH2:23][C:24]1[CH:25]=[N:26][CH:27]=[CH:28][CH:29]=1>>[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[O:12][N:11]=[CH:10][C:9]=2[C:13]([N:18]2[CH2:22][CH2:21][CH2:20][CH:19]2[CH2:23][C:24]2[CH:25]=[N:26][CH:27]=[CH:28][CH:29]=2)=[O:15])=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 179988043-Pyrrolidin-2-ylmethylpyridine dihydrochlorideHCID 228317065-(p-Tolyl)isoxazole-4-carboxylic acid

생성물 1

HCID 248099903-[(1-{[5-(4-Methylphenyl)isoxazol-4-yl]carbonyl}pyrrolidin-2-yl)methyl]pyridine

실험 절차

The title compound was prepared from 5-(4-methylphenyl)isoxazole-4-carboxylic acid (10.2 mg, 0.050 mmol) and 3-pyrrolidin-2-ylmethylpyridine dihydrochloride (14.1 mg, 0.060 mmol) as described in synthetic method B and thereafter purified by preparative HPLC method B to give a solid (4.7 mg). Calcd for C21H21N3O2: 347.1634, found 347.1635.

후처리

  1. custompurified by preparative HPLC method B

출처 및 근거

ORD 기록
ord-aa806dbf174a4201b11bdec21c24bc4e
출처 데이터셋
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07666888B2

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