Triethylamine → 1-[6-(5-Methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridazin-3-yl]-pyrrolidin-2-one

HRID 548829ノート

反応式

HRID 548829 の反応式
[CH3:1][C:2]1[O:6][N:5]=[C:4]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[C:3]=1[CH2:13][O:14][C:15]1[N:20]=[N:19][C:18]([NH2:21])=[CH:17][CH:16]=1.C(N(CC)CC)C.Cl[CH2:30][CH2:31][CH2:32][C:33](Cl)=[O:34]>C1COCC1>[CH3:1][C:2]1[O:6][N:5]=[C:4]([C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=2)[C:3]=1[CH2:13][O:14][C:15]1[N:20]=[N:19][C:18]([N:21]2[CH2:30][CH2:31][CH2:32][C:33]2=[O:34])=[CH:17][CH:16]=1

参加物

5

反応物 3

HCID 8471TriethylamineHCID 783704-Chlorobutyryl chlorideHCID 426297716-(5-Methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridazin-3-ylamine

生成物 1

HCID 426301341-[6-(5-Methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridazin-3-yl]-pyrrolidin-2-one収率 20.4%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a solution of 6-(5-methyl-3-phenyl-isoxazol-4-ylmethoxy)-pyridazin-3-ylamine (1.0 g, 3.5 mmol) in THF (15 ml) was added triethylamine (0.59 mL, 4.3 mmol). The mixture was cooled in an ice bath and a solution of 4-chlorobutyryl chloride (0.48 mL, 4.3 mmol) in THF (5 mL) was added dropwise. After stirring for 1 h at room temperature the precipitate was filtered and the organic phase was evaporated. The residue was dissolved in methanol (20 mL), sodium bicarbonate (1 spatula) was added and the mixture was stirred at room temperature for 1 h. The solvent was evaporated and the residue was extracted (dichloromethane/water). Then the organic phase was dried over sodium sulfate and concentrated. Purification by chromatography (SiO2, heptane/ethyl acetate=100:0 to 60:40) afforded the title compound (250 mg, 20%) (as the most polar component of two formed in the reaction) which was obtained as a white solid. MS: m/e=351.4 [M+H]+.

後処理

  1. temperatureThe mixture was cooled in an ice bath
  2. filtrationwas filtered
  3. customthe organic phase was evaporated
  4. dissolutionThe residue was dissolved in methanol (20 mL)
  5. additionsodium bicarbonate (1 spatula) was added
  6. stirringthe mixture was stirred at room temperature for 1 h
  7. customThe solvent was evaporated
  8. extractionthe residue was extracted (dichloromethane/water)
  9. dry with materialThen the organic phase was dried over sodium sulfate
  10. concentrationconcentrated
  11. customPurification by chromatography (SiO2, heptane/ethyl acetate=100:0 to 60:40)

出典と根拠

ORDレコード
ord-0b5253e42cbc41db9f656dd132679915
出典データセット
uspto-grants-2011_05
特許番号
US07943619B2

反応ノート

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