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Cesium carbonate → methyl {5-[3-(4-cyano-2-propylphenoxy)propoxy]-1H-indol-1-yl}acetate

HRID 734417
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HRID 734417 반응식
[OH:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][C:3]=1[CH2:10][CH2:11][CH3:12].Br[CH2:14][CH2:15][CH2:16][O:17][C:18]1[CH:19]=[C:20]2[C:24](=[CH:25][CH:26]=1)[N:23]([CH2:27][C:28]([O:30][CH3:31])=[O:29])[CH:22]=[CH:21]2.C(=O)([O-])[O-].[Cs+].[Cs+]>CN(C=O)C>[C:6]([C:5]1[CH:8]=[CH:9][C:2]([O:1][CH2:14][CH2:15][CH2:16][O:17][C:18]2[CH:19]=[C:20]3[C:24](=[CH:25][CH:26]=2)[N:23]([CH2:27][C:28]([O:30][CH3:31])=[O:29])[CH:22]=[CH:21]3)=[C:3]([CH2:10][CH2:11][CH3:12])[CH:4]=1)#[N:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 10796Cesium carbonateHCID 139876694-hydroxy-3-propylBenzonitrileHCID 57845410methyl [5-(3-bromopropoxy)-1H-indol-1-yl]acetate

생성물 1

HCID 70971790methyl {5-[3-(4-cyano-2-propylphenoxy)propoxy]-1H-indol-1-yl}acetate수율 23.4%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a mixture of 4-hydroxy-3-propylbenzonitrile (Example 33, 1.33 g, 8.28 mmol) and methyl [5-(3-bromopropoxy)-1H-indol-1-yl]acetate (Example 47, 2.70 g, 8.28 mmol) in DMF (50 mL, containing 1% water), was added cesium carbonate (5.39 g, 16.55 mmol). The mixture was stirred at rt for 24 h and then the solvent was evaporated under reduced pressure. The residue was suspended in ethyl acetate and filtered. The filtrate was concentrated and purified via silica gel column chromatography (0-10% EtOAc in hexanes) to give 787 mg (23%) of the product as a solid. This was used in later steps with no further purification.

후처리

  1. customthe solvent was evaporated under reduced pressure
  2. filtrationfiltered
  3. concentrationThe filtrate was concentrated
  4. custompurified via silica gel column chromatography (0-10% EtOAc in hexanes)

출처 및 근거

ORD 기록
ord-dca313ebc42c44f1a7b7cd1119ebcbcb
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07592361B2

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