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Cesium carbonate → Ethyl 4-(2,4-diamino-3-methoxycarbonylphenyl)-furan-3-carboxylate

HRID 1778403
ノート
印刷プレビュー

反応式

HRID 1778403 の反応式
[NH2:1][C:2]1[C:11](Br)=[CH:10][CH:9]=[C:8]([NH2:13])[C:3]=1[C:4]([O:6][CH3:7])=[O:5].COC([C:18]1[O:19][CH:20]=[CH:21][C:22]=1B(O)O)=O.F[B-](F)(F)F.C([PH+]([C:40]([CH3:43])(C)C)C(C)(C)C)(C)(C)C.[C:44](=O)([O-:46])[O-:45].[Cs+].[Cs+]>O1CCOCC1.O.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd]>[NH2:1][C:2]1[C:3]([C:4]([O:6][CH3:7])=[O:5])=[C:8]([NH2:13])[CH:9]=[CH:10][C:11]=1[C:21]1[C:22]([C:44]([O:46][CH2:40][CH3:43])=[O:45])=[CH:18][O:19][CH:20]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 10796Cesium carbonateHCID 2734635Tri-tert-butylphosphine tetrafluoroborateHCID 66685498[2-(Methoxycarbonyl)furan-3-yl]boronic acidHCID 66685632Methyl 2,6-diamino-3-bromobenzoate2 回

生成物 1

HCID 66685491Ethyl 4-(2,4-diamino-3-methoxycarbonylphenyl)-furan-3-carboxylate収率 689.8%

試薬・触媒・溶媒 3

HCID 9811564Bis(dibenzylideneacetone)palladium触媒
HCID 962Water溶媒
HCID 312751,4-Dioxane溶媒

実験手順

A mixture of methyl 2,6-diamino-3-bromobenzoate (Intermediate 90, 1.0 g), 2-methoxycarbonyl-furan-3-boronic acid (0.980 g), tris-(dibenzylideneacetone)-dipalladium (0.188 g), tri-tert-butylphosphonium tetrafluoroborate (0.119 g) and cesium carbonate (4.0 g) in dioxane (45 mL) and water (6 mL) was de-gassed and flushed with argon. The resultant mixture was stirred at room temperature for 1 hour, then heated at 70° C. for 1 hour. The mixture was cooled, diluted with ethyl acetate and washed with water, dried (MgSO4) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and pentane, with a gradient of 20-50% to give ethyl 4-(2,4-diamino-3-methoxycarbonylphenyl)-furan-3-carboxylate (0.861 g).

後処理

  1. customwas de-gassed
  2. customflushed with argon
  3. temperatureheated at 70° C. for 1 hour
  4. temperatureThe mixture was cooled
  5. additiondiluted with ethyl acetate
  6. washwashed with water
  7. dry with materialdried (MgSO4)
  8. filtrationfiltered
  9. concentrationThe filtrate was concentrated in vacuo
  10. customthe residue was purified by chromatography on silica
  11. washeluting with a mixture of ethyl acetate and pentane, with a gradient of 20-50%

出典と根拠

ORDレコード
ord-52135b162fed41f4b890d3e57a9629fe
出典データセット
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09266896B2

反応ノート

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