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Phenol → 1,3-Dihydro-1-[(3-fluoro-4-pyridinyl)-propylamino]-2H-indol-2-one

HRID 344820
ノート
印刷プレビュー

反応式

HRID 344820 の反応式
[CH2:1]([NH:4][N:5]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH2:7][C:6]1=[O:14])[CH2:2][CH3:3].C1(O)C=CC=CC=1.O.C1(C)C=CC(S(O)(=O)=O)=CC=1.Cl.Cl[C:36]1[CH:41]=[CH:40][N:39]=[CH:38][C:37]=1[F:42].ClC1C=CN=CC=1F.C(=O)(O)[O-].[Na+]>ClCCl>[F:42][C:37]1[CH:38]=[N:39][CH:40]=[CH:41][C:36]=1[N:4]([CH2:1][CH2:2][CH3:3])[N:5]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH2:7][C:6]1=[O:14]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

8

反応物 6

HCID 996PhenolHCID 516892Sodium BicarbonateHCID 521998p-Toluenesulfonic acid monohydrateHCID 38524294-Chloro-3-fluoropyridineHCID 157036281-(Propylamino)-oxindoleHCID 193602344-Chloro-3-fluoropyridine hydrochloride

生成物 1

HCID 14994267
1,3-Dihydro-1-[(3-fluoro-4-pyridinyl)-propylamino]-2H-indol-2-one

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
150 °C

実験手順

To a stirred solution consisting of 1,3-dihydro-1-propylamino-2H-indol-2-one (5.06 g), phenol (13.2 g) and p-toluenesulfonic acid hydrate (0.25 g), heated at 150° C., was added 4-chloro-3-fluoropyridine hydrochloride (5.37 g). Heating was continued at 150° C. for 10.75 hours at which time additional 4-chloro-3-fluoropyridine (2.05 g) was added and heating continued an additional 6.5 hours. Upon cooling to room temperature, the reaction mixture was dissolved in dichloromethane and dilute aqueous sodium bicarbonate. The layers were separated and the organic layer extracted with dilute aqueous sodium bicarbonate (2×). The combined aqueous layers were back-extracted with dichloromethane and ether. The combined organic layers were washed with brine, dried (K2CO3), filtered, and concentrated. Purification via flash column chromatography (silica gel, 2% triethylamine/ether) and another column (silica gel, EtOAc) afforded the desired product as a solid.

後処理

  1. temperatureHeating
  2. additionwas added
  3. temperatureheating
  4. temperatureUpon cooling to room temperature
  5. customThe layers were separated
  6. extractionthe organic layer extracted with dilute aqueous sodium bicarbonate (2×)
  7. extractionThe combined aqueous layers were back-extracted with dichloromethane and ether
  8. washThe combined organic layers were washed with brine
  9. dry with materialdried (K2CO3)
  10. filtrationfiltered
  11. concentrationconcentrated
  12. customPurification via flash column chromatography (silica gel, 2% triethylamine/ether)

出典と根拠

ORDレコード
ord-1e48006d604649abb8cee498f9f8ebae
出典データセット
uspto-grants-1991_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05053511

反応ノート

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