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4-(4-Bromo-3,5-dimethoxyphenyl)-5-methyloxazole → HCID 58432124, 화합물

HRID 1798657
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HRID 1798657 반응식
[Br:1][C:2]1[C:7]([O:8][CH3:9])=[CH:6][C:5]([C:10]2[N:11]=[CH:12][O:13][C:14]=2[CH3:15])=[CH:4][C:3]=1[O:16][CH3:17].CON(C)[C:21](=[O:37])[CH:22]([O:35][CH3:36])[C:23]1[CH:28]=[CH:27][C:26]([N:29]2[CH2:34][CH2:33][O:32][CH2:31][CH2:30]2)=[CH:25][CH:24]=1>>[Br:1][C:2]1[C:7]([O:8][CH3:9])=[CH:6][C:5]([C:10]2[N:11]=[C:12]([C:21](=[O:37])[CH:22]([O:35][CH3:36])[C:23]3[CH:24]=[CH:25][C:26]([N:29]4[CH2:30][CH2:31][O:32][CH2:33][CH2:34]4)=[CH:27][CH:28]=3)[O:13][C:14]=2[CH3:15])=[CH:4][C:3]=1[O:16][CH3:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 584319854-(4-Bromo-3,5-dimethoxyphenyl)-5-methyloxazoleHCID 58431993N,2-dimethoxy-N-methyl-2-(4-morpholinophenyl)acetamide

생성물 1

HCID 58432124HCID 58432124, 화합물

실험 절차

1-(4-(4-Bromo-3,5-dimethoxyphenyl)-5-methyloxazol-2-yl)-2-methoxy-2-(4-morpholinophenyl)ethanone was prepared from 4-(4-bromo-3,5-dimethoxyphenyl)-5-methyloxazole and N,2-dimethoxy-N-methyl-2-(4-morpholinophenyl)acetamide according to the procedure used in Example 30. Purification by chromatography (40% EtOAc-hexanes) gave the product as a yellow solid (0.048 g, 13% yield). MS: m/z 531.1 [M+H]+.

후처리

  1. customPurification by chromatography (40% EtOAc-hexanes)

출처 및 근거

ORD 기록
ord-845a27c73c5d458b9f1afb297d2a7479
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08343970B2

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