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Propargyl bromide → 5-(4-Chloro-phenyl)-2-prop-2-ynyloxy-pyridine

HRID 1916727
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반응식

HRID 1916727 반응식
Br[CH2:2][C:3]#[CH:4].[Cl:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]2[CH:13]=[CH:14][C:15]([OH:18])=[N:16][CH:17]=2)=[CH:8][CH:7]=1.C([O-])([O-])=O.[K+].[K+]>CN(C=O)C>[Cl:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]2[CH:13]=[CH:14][C:15]([O:18][CH2:4][C:3]#[CH:2])=[N:16][CH:17]=2)=[CH:8][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7842Propargyl bromideHCID 11430Potassium CarbonateHCID 178515864HCID 178515864, 화합물

생성물 1

HCID 859696065-(4-Chloro-phenyl)-2-prop-2-ynyloxy-pyridine

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

2 mL (80% in toluene, 18.5 mmol) 3-bromo-propyne are added to a suspension of 3.8 g (18.5 mmol) 5-(4-chloro-phenyl)-pyridin-2-ol and 5.1 g (37 mmol) K2CO3 in 50 mL DMF and the reaction mixture is stirred for 64 h at RT. The mixture is evaporated down i. vac., the residue is combined with 80 mL water, extracted with 150 mL EtOAc and the organic phase is dried over Na2SO4. After the desiccant and solvent have been eliminated the residue is purified by chromatography (silica gel, cyc/EtOAc 2:1).

후처리

  1. customThe mixture is evaporated down i
  2. extractionextracted with 150 mL EtOAc
  3. dry with materialthe organic phase is dried over Na2SO4
  4. customis purified by chromatography (silica gel, cyc/EtOAc 2:1)

출처 및 근거

ORD 기록
ord-2fbb8cdabd9e41b390e925e98188f3c7
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08618132B2

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