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Dimethylformamide → HCID 69055376, 화합물

HRID 1727221
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HRID 1727221 반응식
[H-].[Na+].CN(C)C=O.[OH:8][CH:9]1[CH2:14][CH2:13][CH2:12][N:11]([C:15]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16])[CH2:10]1.[F:22][C:23]1[CH:24]=[C:25]([CH:28]=[CH:29][C:30]=1[F:31])[CH2:26]Br>CCCCC>[F:22][C:23]1[CH:24]=[C:25]([CH2:26][O:8][CH:9]2[CH2:14][CH2:13][CH2:12][N:11]([C:15]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16])[CH2:10]2)[CH:28]=[CH:29][C:30]=1[F:31]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6228DimethylformamideHCID 24758Sodium hydrideHCID 5456991-Boc-3-hydroxypiperidineHCID 5814364-(Bromomethyl)-1,2-difluorobenzene

생성물 1

HCID 69055376HCID 69055376, 화합물수율 94%

시약·촉매·용매 1

HCID 8003Pentane용매

실험 절차

To sodium hydride (60% w/w dispersion in oil, 0.62 g, 16.4 mmol) washed in pentane was added N,N-dimethylformamide (20 ml) and then 1,1-dimethylethyl 3-hydroxypiperidine-1-carboxylate (Preparation 117, 3.0 g, 14.9 mmol). The reaction mixture was stirred for 1 h, before adding 3,4-difluorobenzyl bromide (2.0 ml, 16.4 mmol) and stirring the reaction mixture for 18 h. The reaction mixture was concentrated in vacuo and the crude residue was dissolved in dichloromethane and washed with brine and dried (MgSO4) before concentrating in vacuo. The crude residue was purified by flash chromatography to give the title compound (4.58 g, 94%).

후처리

  1. stirringstirring the reaction mixture for 18 h
  2. concentrationThe reaction mixture was concentrated in vacuo
  3. dissolutionthe crude residue was dissolved in dichloromethane
  4. washwashed with brine
  5. dry with materialdried (MgSO4)
  6. concentrationbefore concentrating in vacuo
  7. customThe crude residue was purified by flash chromatography

출처 및 근거

ORD 기록
ord-b11729271d4243d9840bb77d6af73ac2
출처 데이터셋
uspto-grants-2009_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07494992B2

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