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

HRID 734417
ノート
印刷プレビュー

反応式

HRID 734417 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-dca313ebc42c44f1a7b7cd1119ebcbcb
出典データセット
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07592361B2

反応ノート

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