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Dimethyl Sulfoxide → Ethyl 4-[(4-(2-pyridyloxy)phenyl)methyl]piperazinecarboxylate

HRID 902104
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반응식

HRID 902104 반응식
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[O:7][C:8]1[CH:13]=[CH:12][C:11]([CH2:14]Cl)=[CH:10][CH:9]=1.[N:16]1([C:22]([O:24][CH2:25][CH3:26])=[O:23])[CH2:21][CH2:20][NH:19][CH2:18][CH2:17]1.CS(C)=O>>[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[O:7][C:8]1[CH:13]=[CH:12][C:11]([CH2:14][N:19]2[CH2:18][CH2:17][N:16]([C:22]([O:24][CH2:25][CH3:26])=[O:23])[CH2:21][CH2:20]2)=[CH:10][CH:9]=1
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참가 물질

4

반응물 3

HCID 679Dimethyl SulfoxideHCID 84311-Piperazinecarboxylic acid, ethyl esterHCID 22292927(4-(2-Pyridyloxy)phenyl)methyl chloride

생성물 1

HCID 69313800Ethyl 4-[(4-(2-pyridyloxy)phenyl)methyl]piperazinecarboxylate수율 99.6%

실험 절차

This compound was prepared in a manner analogous to that of Example 2, Step D, using 2.2 grams (0.010 mole) of 4-(2-pyridyloxy)phenylmethyl chloride, 1.6 grams (0.010 mole) of ethyl 1-piperazinecarboxylate, and 3.9 grams (0.030 mole) of DMSO, yielding 3.4 grams of the subject compound. The NMR spectrum was consistent with the proposed structure.

후처리

  1. customThis compound was prepared in a manner analogous to that of Example 2, Step D

출처 및 근거

ORD 기록
ord-2befccb730454675af5533859ae23946
출처 데이터셋
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07365082B2

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