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Dichloromethane → 4-Phenyl-1-{[3-(trifluoromethyl)[1,2,4]triazolo[4,3-b]pyridazin-7-yl]methyl}pyrrolidin-2-one

HRID 2043688
ノート
印刷プレビュー

反応式

HRID 2043688 の反応式
Cl.[NH2:2][CH2:3][CH:4]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[CH2:5][C:6]([O:8]C)=O.[F:16][C:17]([F:30])([F:29])[C:18]1[N:22]2[N:23]=[CH:24][C:25]([CH:27]=O)=[CH:26][C:21]2=[N:20][N:19]=1.C(N(CC)CC)C.ClCCl>ClC(Cl)C.COCCOC>[C:10]1([CH:4]2[CH2:3][N:2]([CH2:27][C:25]3[CH:24]=[N:23][N:22]4[C:18]([C:17]([F:30])([F:16])[F:29])=[N:19][N:20]=[C:21]4[CH:26]=3)[C:6](=[O:8])[CH2:5]2)[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=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 6344DichloromethaneHCID 8471TriethylamineHCID 536292043-(Trifluoromethyl)[1,2,4]triazolo[4,3-b]pyridazine-7-carbaldehydeHCID 68748102Methyl 4-amino-3-phenylbutanoate hydrochloride

生成物 1

HCID 577430604-Phenyl-1-{[3-(trifluoromethyl)[1,2,4]triazolo[4,3-b]pyridazin-7-yl]methyl}pyrrolidin-2-one収率 36%

試薬・触媒・溶媒 2

HCID 63651,1-Dichloroethane溶媒
HCID 80711,2-Dimethoxyethane溶媒

反応条件

温度
11 °C

実験手順

Methyl 4-amino-3-phenylbutanoate hydrochloride x11 (0.19 g, 0.83 mmol, 1.05 eq) is added to a solution of aldehyde x235 (0.17 g, 0.79 mmol) in dry dichloroethane (DCE) (7.8 ml). The mixture is kept at room temperature for 30 min, cooled to 10-12° C., and a solution of triethylamine (0.15 ml, 0.83 mmol, 1.05 eq) in dry DME (2.5 ml) is added dropwise. The mixture is additionally stirred at the same temperature for 1 h and cooled to 0-5° C. Then STAB (0.23 g, 1.10 mmol, 1.4 eq) is added in portions under vigorous stirring. The mixture is additionally stirred at 0-5° C. for 30 min and kept at room temperature overnight. Then the mixture is heated to 60° C. for 2 h and cooled to room temperature. An equal volume of dichloromethane is added, and the mixture is washed with 10% K2CO3 (2×10 ml). The mixture is dried over anhydrous Na2SO4 and evaporated. The oily residue is triturated with ether, and the formed crystals are separated by filtration, washed twice with ether, and vacuum-dried to give white fine-crystalline 4-phenyl-1-{[3-(trifluoromethyl)[1,2,4]triazolo[4,3-b]pyridazin-7-yl]methyl}pyrrolidin-2-one 255.

後処理

  1. temperaturecooled to 0-5° C
  2. additionThen STAB (0.23 g, 1.10 mmol, 1.4 eq) is added in portions under vigorous stirring
  3. stirringThe mixture is additionally stirred at 0-5° C. for 30 min
  4. waitkept at room temperature overnight
  5. temperatureThen the mixture is heated to 60° C. for 2 h
  6. temperaturecooled to room temperature
  7. washthe mixture is washed with 10% K2CO3 (2×10 ml)
  8. dry with materialThe mixture is dried over anhydrous Na2SO4
  9. customevaporated
  10. customThe oily residue is triturated with ether
  11. customthe formed crystals are separated by filtration
  12. washwashed twice with ether
  13. customvacuum-dried

出典と根拠

ORDレコード
ord-722b5906cf88408cac3effb8bac4cc67
出典データセット
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08586623B2

反応ノート

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