Sodium Chloride → (3-Morpholin-4-yl-phenyl)-pyrrolo[2,1-f][1,2,4]triazin-2-yl-amine

HRID 1261938ノート

反応式

HRID 1261938 の反応式
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.Br[C:21]1[N:29]2[C:24]([CH:25]=[N:26][C:27]([NH:30][C:31]3[CH:36]=[CH:35][CH:34]=[C:33]([N:37]4[CH2:42][CH2:41][O:40][CH2:39][CH2:38]4)[CH:32]=3)=[N:28]2)=[CH:23][CH:22]=1.ClC1C=CC(C(F)(F)F)=CC=1B(O)O.C(=O)([O-])[O-].[Na+].[Na+].[Cl-].[Na+]>O1CCCC1.O.C(O)C.C([O-])(=O)C.[Pd+2].N1(C2C=C(NC3N=CC4=CC=CN4N=3)C=CC=2)CCOCC1.C([O-])(=O)C>[N:37]1([C:33]2[CH:32]=[C:31]([NH:30][C:27]3[N:26]=[CH:25][C:24]4=[CH:23][CH:22]=[CH:21][N:29]4[N:28]=3)[CH:36]=[CH:35][CH:34]=2)[CH2:38][CH2:39][O:40][CH2:41][CH2:42]1

参加物

10

反応物 5

HCID 5234Sodium ChlorideHCID 10340Sodium CarbonateHCID 11776TriphenylphosphineHCID 27826702-Chloro-5-(trifluoromethyl)phenylboronic acidHCID 66711115(7-Bromo-pyrrolo[2,1-f][1,2,4]triazin-2-yl)-(3-morpholin-4-yl-phenyl)-amine

生成物 1

HCID 66711030(3-Morpholin-4-yl-phenyl)-pyrrolo[2,1-f][1,2,4]triazin-2-yl-amine

試薬・触媒・溶媒 4

HCID 86661665HCID 86661665、化合物触媒HCID 702Ethanol溶媒HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

(3-Morpholin-4-yl-phenyl)-pyrrolo[2,1-f][1,2,4]triazin-2-yl-amine Palladium Acetate (0.029 g, 0.00013 mol) and Triphenylphosphine (0.042 g, 0.00016 mol) were dissolved in Tetrahydrofuran (2.0 mL) and the mixture was allowed to stir at room temperature for 10 minutes. (7-Bromo-pyrrolo[2,1-f][1,2,4]triazin-2-yl)-(3-morpholin-4-yl-phenyl)-amine (0.240 g, 0.000641 mol) was then added and the reaction was again allowed to stir for 10 minutes. 2-chloro-5-trifluoromethylphenylboronic acid (0.288 g, 0.00128 mol) was added followed by 0.9 M of Sodium carbonate in water (2 mL) and Ethanol (2.0 mL). The reaction mixture was then heated at 80° C. and was allowed to stir overnight. The reaction mixture was poured over saturated sodium chloride, and organics were extracted with ethyl acetate/dichloromethane. Combined organics were dried over sodium sulfate, filtered and reduced en vacuo. Because the desired product was not formed, 22.96 mg of (3-Morpholin-4-yl-phenyl)-pyrrolo[2,1-f][1,2,4]triazin-2-yl-amine was purified by Gilson prep HPLC as a byproduct. (M+H)=296.14. 1H NMR (400 MHz, CDCl3) δ 9.47 (s, 1H), 8.62 (s, 1H), 7.98 (s, 1H), 7.88 (s, 1H), 7.36 (m, 2H), 7.08 (d, 1H, J=4.85 Hz), 6.91 (m, 2H), 4.02 (m, 4H), 3.41 (m, 2H).

後処理

  1. stirringto stir for 10 minutes
  2. temperatureThe reaction mixture was then heated at 80° C.
  3. stirringto stir overnight
  4. extractionorganics were extracted with ethyl acetate/dichloromethane
  5. dry with materialCombined organics were dried over sodium sulfate
  6. filtrationfiltered

出典と根拠

ORDレコード
ord-0c35452c2d474025844c3d415297d887
出典データセット
uspto-grants-2013_06
特許番号
US08471005B2

反応ノート

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