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Cesium carbonate → 3-(6-chloro-8-oxo-8,9-dihydro-7H-purin-2-ylamino)-4-nitrobenzonitrile

HRID 600438
ノート
印刷プレビュー

反応式

HRID 600438 の反応式
[NH2:1][C:2]1[N:10]=[C:9]2[C:5]([NH:6][C:7](=[O:11])[NH:8]2)=[C:4]([Cl:12])[N:3]=1.C([O-])([O-])=O.[Cs+].[Cs+].Br[C:20]1[CH:21]=[C:22]([CH:25]=[CH:26][C:27]=1[N+:28]([O-:30])=[O:29])[C:23]#[N:24].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>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].C(O)C.O1CCOCC1>[Cl:12][C:4]1[N:3]=[C:2]([NH:1][C:26]2[CH:25]=[C:22]([CH:21]=[CH:20][C:27]=2[N+:28]([O-:30])=[O:29])[C:23]#[N:24])[N:10]=[C:9]2[C:5]=1[NH:6][C:7](=[O:11])[NH:8]2
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 6360441,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 184132163-Bromo-4-nitrobenzonitrileHCID 576126262-amino-6-chloro-7H-purin-8(9H)-one

生成物 1

HCID 576127083-(6-chloro-8-oxo-8,9-dihydro-7H-purin-2-ylamino)-4-nitrobenzonitrile収率 46%

試薬・触媒・溶媒 3

HCID 9811564Bis(dibenzylideneacetone)palladium触媒HCID 702Ethanol溶媒HCID 312751,4-Dioxane溶媒

実験手順

To an oven-dried microwave flask under Ar was added 2-amino-6-chloro-7H-purin-8(9H)-one (0.64 g, 3.46 mmol, 1.0 equiv.) followed by anhydrous dioxane (10 mL) and anhydrous ethanol (4 mL); Cs2CO3 (Aldrich, 2.25 g, 6.92 mmol, 2 equiv.), 3-bromo-4-nitro-benzonitrile (1.02 g, 4.5 mmol, 1.3 equiv.), Xantphos (Strem, 0.6 g, 1.04 mmol, 0.3 equiv.) and Pd2(dba)3 (Strem, 0.32 g, 0.35 mmol, 0.1 equiv.) were all added as solids, and the mixture was stirred under Ar, at room temperature for 3 min. The flask was capped and heated in the microwave at 140° C. for 150 min (LC-MS shows reaction to be complete). The reaction mixture was cooled to room temperature, then concentrated in vacuo to give a dark brown residue, which was purified by flash chromatography (silica gel, gradual elution 3/1 ethyl acetate/hexanes, then 4/1 ethyl acetate/hexanes with 1% MeOH to 20% MeOH) to give the desired product as an orange solid in 46% yield. 1H NMR (300 MHz, CD3COOD) δ, ppm: 9.31 (d, 1H), 8.36 (d, 1H), 7.43 (dd, 1H); MS (EI) m/z 332.0 (MH)+.

後処理

  1. additionall added as solids
  2. customThe flask was capped
  3. temperatureheated in the microwave at 140° C. for 150 min
  4. custom(LC-MS shows reaction to be complete)
  5. temperatureThe reaction mixture was cooled to room temperature
  6. concentrationconcentrated in vacuo
  7. customto give a dark brown residue, which
  8. customwas purified by flash chromatography (
  9. washsilica gel, gradual elution 3/1 ethyl acetate/hexanes

出典と根拠

ORDレコード
ord-4cfc335002ba411586767c12a6b6bdd2
出典データセット
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07902187B2

反応ノート

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