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Tetrahydrofuran → HCID 59406980, 화합물

HRID 589926
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HRID 589926 반응식
[Si]([O:8][CH2:9][C:10]1[CH:11]=[CH:12][C:13]([C:16]2(CC(N)=O)[CH2:18][CH2:17]2)=[N:14][CH:15]=1)(C(C)(C)C)(C)C.[F-].[CH2:24]([N+:28](CCCC)(CCCC)CCCC)[CH2:25]CC.[O:41]1CCCC1>>[OH:8][CH2:9][C:10]1[CH:11]=[CH:12][C:13]([C:16]2([NH:28][C:24](=[O:41])[CH3:25])[CH2:17][CH2:18]2)=[N:14][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 8028Tetrahydrofuran2회HCID 2724141Tetrabutylammonium FluorideHCID 684316481-[5-(Tert-butyldimethylsilanyloxymethyl)pyridin-2-yl]cyclopropylacetamide

생성물 1

HCID 59406980HCID 59406980, 화합물

실험 절차

1-[5-(tert-Butyldimethylsilanyloxymethyl)pyridin-2-yl]cyclopropylacetamide (156 mg) was dissolved in tetrahydrofuran (2 ml), and a solution (1 mol/l, 1.46 ml) of tetrabutylammonium fluoride in tetrahydrofuran was added thereto. The mixture was stirred at room temperature for 25 min. The solvent was evaporated and the obtained residue was purified by column chromatography (Yamazen HI-FLASH™ COLUMN size L, elution solvent: ethyl acetate/methanol) to give the title compound (109 mg).

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. customThe solvent was evaporated
  2. customthe obtained residue was purified by column chromatography (Yamazen HI-FLASH™ COLUMN size L, elution solvent: ethyl acetate/methanol)

출처 및 근거

ORD 기록
ord-5b981364ca3b42f5a7c56553cef4f7bf
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09233969B2

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