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3-Aminopyridine → 5-[2-(Pyridin-3-ylamino)-pyrimidin-4-yl]-thiophene-2-carboxylic acid ethyl ester

HRID 1012185
ノート
印刷プレビュー

反応式

HRID 1012185 の反応式
CC1(C)C2C(=C(P(C3C=CC=CC=3)C3C=CC=CC=3)C=CC=2)OC2C(P(C3C=CC=CC=3)C3C=CC=CC=3)=CC=CC1=2.C(=O)([O-])[O-].[K+].[K+].[CH2:49]([O:51][C:52]([C:54]1[S:55][C:56]([C:59]2[CH:64]=[CH:63][N:62]=[C:61](Cl)[N:60]=2)=[CH:57][CH:58]=1)=[O:53])[CH3:50].[NH2:66][C:67]1[CH:68]=[N:69][CH:70]=[CH:71][CH:72]=1>O1CCOCC1.CCOC(C)=O.O.CC(O)=O.CC(O)=O.[Pd]>[CH2:49]([O:51][C:52]([C:54]1[S:55][C:56]([C:59]2[CH:64]=[CH:63][N:62]=[C:61]([NH:66][C:67]3[CH:68]=[N:69][CH:70]=[CH:71][CH:72]=3)[N:60]=2)=[CH:57][CH:58]=1)=[O:53])[CH3:50]
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

9

反応物 4

HCID 100093-AminopyridineHCID 11430Potassium CarbonateHCID 6360441,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 594684545-(2-Chloro-pyrimidin-4-yl)-thiophene-2-carboxylic acid ethyl ester

生成物 1

HCID 594686225-[2-(Pyridin-3-ylamino)-pyrimidin-4-yl]-thiophene-2-carboxylic acid ethyl ester収率 62.4%

試薬・触媒・溶媒

4
HCID 4144353Palladium (II) acetate触媒HCID 962Water溶媒HCID 8857Ethyl Acetate溶媒HCID 312751,4-Dioxane溶媒2 回

反応条件

温度
100 °C

実験手順

Palladium II acetate (8.3 mg, 0.1 mmol) and xantphos 42.8 mg, 0.2 mmol) were precombined in 4 mL dry dioxane under nitrogen gas. Potassium carbonate (1.03 g, 7.46 mmol) was added followed by a solution of 5-(2-Chloro-pyrimidin-4-yl)-thiophene-2-carboxylic acid ethyl ester (100 mg, 0.373 mmol) and 3-aminopyridine (42 mg, 0.447 mmol) in 3 mL dioxane. The reaction was heated in a capped vial at 100° C. for 20 h. The cooled reaction mixture was diluted with EtOAc and water and the layers were separated. The organic layer was dried over Na2SO4 and concentrated in vacuo. The residue was redissolved in ethyl ether and treated with 2 M HCl in ether to generate a precipitate which was collected by filtration to afford 76 mg (56.3%) of the title compound. The crude material was used in the next step.

後処理

  1. customThe cooled reaction mixture
  2. customthe layers were separated
  3. dry with materialThe organic layer was dried over Na2SO4
  4. concentrationconcentrated in vacuo
  5. dissolutionThe residue was redissolved in ethyl ether
  6. additiontreated with 2 M HCl in ether
  7. filtrationwas collected by filtration

出典と根拠

ORDレコード
ord-dc23e332563f4fb4bbb05c3fd47ca62e
出典データセット
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07977481B2

反応ノート

読み込み中…

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