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Dimethylformamide → 1-(4-Chlorobenzyl)-3-(2-(3-pyridyl)ethenyl)-5-(2-quinolylmethoxy)indole

HRID 486060
ノート
印刷プレビュー

反応式

HRID 486060 の反応式
[H-].[Na+].[Cl-].[N:4]1[CH:9]=[CH:8][CH:7]=[C:6]([CH2:10][P+](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[CH:5]=1.CN(C)C=O.[Cl:35][C:36]1[CH:65]=[CH:64][C:39]([CH2:40][N:41]2[C:49]3[C:44](=[CH:45][C:46]([O:50][CH2:51][C:52]4[CH:61]=[CH:60][C:59]5[C:54](=[CH:55][CH:56]=[CH:57][CH:58]=5)[N:53]=4)=[CH:47][CH:48]=3)[C:43]([CH:62]=O)=[CH:42]2)=[CH:38][CH:37]=1>O.C(OCC)(=O)C>[Cl:35][C:36]1[CH:37]=[CH:38][C:39]([CH2:40][N:41]2[C:49]3[C:44](=[CH:45][C:46]([O:50][CH2:51][C:52]4[CH:61]=[CH:60][C:59]5[C:54](=[CH:55][CH:56]=[CH:57][CH:58]=5)[N:53]=4)=[CH:47][CH:48]=3)[C:43]([CH:62]=[CH:10][C:6]3[CH:5]=[N:4][CH:9]=[CH:8][CH:7]=3)=[CH:42]2)=[CH:64][CH:65]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 6228DimethylformamideHCID 24758Sodium hydrideHCID 190973381-(4-Chlorobenzyl)-3-formyl-5-(2-quinolylmethoxy)indoleHCID 22325077Triphenyl(3-pyridylmethyl)phosphonium chloride

生成物 1

HCID 545011021-(4-Chlorobenzyl)-3-(2-(3-pyridyl)ethenyl)-5-(2-quinolylmethoxy)indole収率 30.5%

試薬・触媒・溶媒 1

HCID 22728543Water ethylacetate溶媒

実験手順

A suspension of sodium hydride (60%-oil suspension, 0.39 g), 3-picolyl-triphenylphosphonium chloride (2.55 g) and N,N-dimethylformamide was stirred for 20 minutes, followed by the addition of 1-(4-chlorobenzyl)-3-formyl-5-(2-quinolylmethoxy)indole (3.0 g). The mixture was stirred for an additional 10 hours and then poured into water-ethyl acetate (50% v/v). The organic layer was separated, washed with brine, dried over magnesium sulfate, and concentrated in vacuo. The resultant crude product was purified by chromatography on silica gel using 50%-ethyl acetate in n-hexanes as eluent to yield 1-(4-chlorobenzyl)-3-(2-(3-pyridyl)ethenyl)-5-(2-quinolylmethoxy)indole (1.0 g), m.p. 169°-171° C.

後処理

  1. stirringThe mixture was stirred for an additional 10 hours
  2. customThe organic layer was separated
  3. washwashed with brine
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated in vacuo
  6. customThe resultant crude product was purified by chromatography on silica gel using 50%-ethyl acetate in n-hexanes as eluent

出典と根拠

ORDレコード
ord-6430d7dc8c0b4b4dba5c96136a706f3d
出典データセット
uspto-grants-1994_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05290788

反応ノート

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