Iodoethane → 3-Benzyloxy-1-ethyl-5,6,8-trifluoro-7-pyrrolidin-1-yl-1H-quinazoline-2,4-dione

HRID 2416855ノート

反応式

HRID 2416855 の反応式
[CH2:1]([O:8][N:9]1[C:18](=[O:19])[C:17]2[C:12](=[C:13]([F:23])[C:14](F)=[C:15]([F:21])[C:16]=2[F:20])[NH:11][C:10]1=[O:24])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH:25]1[CH2:29][CH2:28][CH2:27][CH2:26]1.[CH2:30](I)[CH3:31].[H-].[Na+]>CC(N(C)C)=O.CN(C=O)C>[CH2:1]([O:8][N:9]1[C:18](=[O:19])[C:17]2[C:12](=[C:13]([F:23])[C:14]([N:25]3[CH2:29][CH2:28][CH2:27][CH2:26]3)=[C:15]([F:21])[C:16]=2[F:20])[N:11]([CH2:30][CH3:31])[C:10]1=[O:24])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

7

反応物 4

HCID 6340IodoethaneHCID 24758Sodium hydrideHCID 31268PyrrolidineHCID 226328803-Benzyloxy-5,6,7,8-tetrafluoro-1H-quinazoline-2,4-dione

生成物 1

HCID 226329973-Benzyloxy-1-ethyl-5,6,8-trifluoro-7-pyrrolidin-1-yl-1H-quinazoline-2,4-dione収率 22.1%

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 31374Dimethylacetamide溶媒

反応条件

温度
60 °C

実験手順

A solution of 3-benzyloxy-5,6,7,8-tetrafluoro-1H-quinazoline-2,4-dione (Example W-3, 0.90 g, 2.7 mmol), in DMA (10 mL) was reacted with pyrrolidine (0.55 mL, 6.6 mmol) and heated to 60° C. for 3 hours. The mixture was then cooled and quenched with H2O and acidified with citric acid. The mixture was then extracted with ethyl acetate, dried with MgSO4, and concentrated. The residue was triturated with diethyl ether/hexanes and the solid filtered and dried (0.87 g). A portion of the solid (0.500 g, 1.28 mmol) was dissolved in DMF and reacted with ethyl iodide (1.0 mL, 12.77 mmol) and sodium hydride (0.060 g, 1.5 mmol). The mixture was stirred for 16 hours. The mixture was quenched with H2O and extracted with ethyl acetate. The organic layers were combined, dried with sodium sulfate. and concentrated. The residue was triturated with diethyl ether and filtered to yield 0.25 g of the title compound as a solid.

後処理

  1. temperatureThe mixture was then cooled
  2. customquenched with H2O
  3. extractionThe mixture was then extracted with ethyl acetate
  4. dry with materialdried with MgSO4
  5. concentrationconcentrated
  6. customThe residue was triturated with diethyl ether/hexanes
  7. filtrationthe solid filtered
  8. customdried (0.87 g)
  9. customThe mixture was quenched with H2O
  10. extractionextracted with ethyl acetate
  11. dry with materialdried with sodium sulfate
  12. concentrationand concentrated
  13. customThe residue was triturated with diethyl ether
  14. filtrationfiltered

出典と根拠

ORDレコード
ord-3dacb974c1d545168bd9b2aa9a893a08
出典データセット
uspto-grants-2004_11
特許番号
US06825199B2

反応ノート

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