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Benzophenone imine → Benzhydrylidene-[4-(2-ethyl-5,7-dimethyl-pyrazolo[1,5-a]pyrimidin-3-ylmethyl)-phenyl]-amine

HRID 403489
ノート
印刷プレビュー

反応式

HRID 403489 の反応式
[C:1]1([C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[NH:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C1C=CC(P(C2C(C3C(P(C4C=CC=CC=4)C4C=CC=CC=4)=CC=C4C=3C=CC=C4)=C3C(C=CC=C3)=CC=2)C2C=CC=CC=2)=CC=1.CC(C)([O-])C.[Na+].Br[C:68]1[CH:87]=[CH:86][C:71]([CH2:72][C:73]2[C:74]([CH2:84][CH3:85])=[N:75][N:76]3[C:81]([CH3:82])=[CH:80][C:79]([CH3:83])=[N:78][C:77]=23)=[CH:70][CH:69]=1>C1(C)C=CC=CC=1.C([O-])(=O)C.C([O-])(=O)C.[Pd+2]>[C:7](=[N:8][C:68]1[CH:87]=[CH:86][C:71]([CH2:72][C:73]2[C:74]([CH2:84][CH3:85])=[N:75][N:76]3[C:81]([CH3:82])=[CH:80][C:79]([CH3:83])=[N:78][C:77]=23)=[CH:70][CH:69]=1)([C:1]1[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1)[C:9]1[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=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 4

HCID 136809Benzophenone imineHCID 634876Binap, (A+-)-HCID 23676156Sodium t-butoxideHCID 683789033-(4-Bromobenzyl)-2-ethyl-5,7-dimethylpyrazolo[1,5-A]pyrimidine

生成物 1

HCID 86671753Benzhydrylidene-[4-(2-ethyl-5,7-dimethyl-pyrazolo[1,5-a]pyrimidin-3-ylmethyl)-phenyl]-amine

試薬・触媒・溶媒 2

HCID 167845
palladium(II) acetate
触媒
HCID 1140Toluene溶媒

反応条件

温度
105 °C

実験手順

Diphenylmethanimine (7.53 g, 39.5 mmol), BINAP (447 mg, 0.718 mmol) and sodium tert-butoxide (6.9 g, 71.8 mmol) were dissolved in 100 ml of toluene. The reaction mixture was heated to 105° C. and stirred for 5 min. Then 3-(4-bromo-benzyl)-2-ethyl-5,7-dimethyl-pyrazolo[1,5-a]pyrimidine (3) (13 g, 35.9 mmol) and palladium diacetate (81 mg, 0.36 mmol) were added and the reaction mixture was stirred for 12 h at 110° C. The organic layer was extracted two times with EtOAc, washed with water and brine, dried over Na2 SO4 and concentrated under reduced pressure. The precipitate was suspended in cyclohexane and filtered to afford a beige solid.

後処理

  1. stirringthe reaction mixture was stirred for 12 h at 110° C
  2. extractionThe organic layer was extracted two times with EtOAc
  3. washwashed with water and brine
  4. customdried over Na2 SO4
  5. concentrationconcentrated under reduced pressure
  6. filtrationfiltered
  7. customto afford a beige solid

出典と根拠

ORDレコード
ord-42e29716b9e84fa9b9a7884c95b1a570
出典データセット
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08748435B2

反応ノート

読み込み中…

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