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1,2-Dimethoxyethane → (R)-4-((R)-1-(3-methyl-6-(4-(piperazin-1-yl)phenyl)-3H-imidazo[4,5-c]pyridin-4-yloxy)ethyl)pyrrolidin-2-one

HRID 2209046
ノート
印刷プレビュー

反応式

HRID 2209046 の反応式
Cl[C:2]1[N:7]=[C:6]([O:8][C@@H:9]([C@H:11]2[CH2:15][NH:14][C:13](=[O:16])[CH2:12]2)[CH3:10])[C:5]2[N:17]([CH3:20])[CH:18]=[N:19][C:4]=2[CH:3]=1.O[C@@H]([C@H]1CN([C@@H]([C:31]2[CH:36]=[CH:35][C:34](OC)=[CH:33][CH:32]=2)C)C(=O)C1)C.B(O)O.C(=O)([O-])[O-].[Cs+].[Cs+].CO[CH2:51][CH2:52]OC>O>[CH3:20][N:17]1[C:5]2[C:6]([O:8][C@@H:9]([C@H:11]3[CH2:15][NH:14][C:13](=[O:16])[CH2:12]3)[CH3:10])=[N:7][C:2]([C:31]3[CH:32]=[CH:33][C:34]([N:7]4[CH2:52][CH2:51][NH:17][CH2:5][CH2:6]4)=[CH:35][CH:36]=3)=[CH:3][C:4]=2[N:19]=[CH:18]1
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

7

反応物 5

HCID 80711,2-DimethoxyethaneHCID 10796Cesium carbonateHCID 61668Boronic AcidHCID 117843294(R)-4-((R)-1-((6-chloro-3-methyl-3H-imidazo[4,5-c]pyridin-4-yl)oxy)ethyl)pyrrolidin-2-oneHCID 117843967(R)-4-((R)-1-hydroxyethyl)-1-((R)-1-(4-methoxyphenyl)ethyl)pyrrolidin-2-one

生成物 1

HCID 117844142
(R)-4-((R)-1-(3-methyl-6-(4-(piperazin-1-yl)phenyl)-3H-imidazo[4,5-c]pyridin-4-yloxy)ethyl)pyrrolidin-2-one

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
100 °C

実験手順

To an appropriate sized container charged with a magnetic stir bar, aryl halide 2.06, 2.58 or 2.62 (1 equiv), boronic acid or ester (1.2 equiv), cesium carbonate (3 equiv), and PEPPSI-IPr catalyst (0.1 equiv) were added and reagents were taken up in 2:1 DME:water. After evacuating and backfilling with argon, mixture was heated at 100° C. for one hour. After cooling to room temperature, mixture is poured into water and extracted with ethyl acetate. Combined organics were dried, filtered, and concentrated under reduced pressure and resulting residues were purified by silica gel column chromatography or reverse phase HPLC to yield Examples 3B.01-3B.31.

後処理

  1. additionTo an appropriate sized container charged with a magnetic stir bar
  2. customAfter evacuating
  3. temperatureAfter cooling to room temperature
  4. additionmixture is poured into water
  5. extractionextracted with ethyl acetate
  6. customCombined organics were dried
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure
  9. customresulting residues
  10. customwere purified by silica gel column chromatography
  11. customto yield Examples 3B.01-3B.31

出典と根拠

ORDレコード
ord-9152d15721ab47f2b83dc397703c2a28
出典データセット
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09376441B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート