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2-[6-[(6-Bromohexyl)oxy]-1-hexynyl]-4-pyridinecarboxamide → 2-[6-[(6-Bromohexyl)oxy]hexyl]-4-pyridinecarboxamide

HRID 1649792
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인쇄 미리보기

반응식

HRID 1649792 반응식
[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][O:8][CH2:9][CH2:10][CH2:11][CH2:12][C:13]#[C:14][C:15]1[CH:20]=[C:19]([C:21]([NH2:23])=[O:22])[CH:18]=[CH:17][N:16]=1>C(O)C.[Pd]=O>[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][O:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][C:15]1[CH:20]=[C:19]([C:21]([NH2:23])=[O:22])[CH:18]=[CH:17][N:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 198547972-[6-[(6-Bromohexyl)oxy]-1-hexynyl]-4-pyridinecarboxamide

생성물 1

HCID 198547862-[6-[(6-Bromohexyl)oxy]hexyl]-4-pyridinecarboxamide수율 99.9%

시약·촉매·용매 2

HCID 5083724Palladium monoxide촉매HCID 702Ethanol용매

실험 절차

A solution of 2-[6-[(6-bromohexyl)oxy]-1-hexynyl]-4-pyridinecarboxamide (1.04 g) in ethanol (20 ml) was hydrogenated over pre-hydrogenated 10% palladium oxide on carbon (50% aqueous paste, 115 mg). The mixture was filtered through hyflo and the filtrate evaporated to give the title compound as a pale yellow solid (1.05 g), m.p. 73°-75°.

후처리

  1. filtrationThe mixture was filtered through hyflo
  2. customthe filtrate evaporated

출처 및 근거

ORD 기록
ord-ce659111ba0a4b869bef6c18c9e22d7d
출처 데이터셋
uspto-grants-1990_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04921867

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