Borane;tetrahydrofuran → 1-Cyclopropyl-1,2,3,4-tetrahydroquinoxaline

HRID 1025822

反応式

HRID 1025822 の反応式
[CH:1]1([N:4]2[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[NH:7][C:6](=O)[C:5]2=O)[CH2:3][CH2:2]1.B.O1CCCC1>O1CCCC1>[CH:1]1([N:4]2[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[NH:7][CH2:6][CH2:5]2)[CH2:3][CH2:2]1

参加物

4

反応物 2

HCID 2723981Borane;tetrahydrofuranHCID 212796951-Cyclopropyl-1,4-dihydroquinoxaline-2,3-dione

生成物 1

HCID 673207551-Cyclopropyl-1,2,3,4-tetrahydroquinoxaline収率 49%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a stirred suspension of 1-cyclopropyl-1,4-dihydro-quinoxaline-2,3-dione (10.0 g, 49.45 mmol, 1.0 equiv) in tetrahydrofuran (500 mL) was added dropwise a 1 M solution of borane-tetrahydrofuran complex (108.8 mL, 108.8 mmol, 2.2 equiv; [CAS RN 14044-65-6]) and the reaction mixture stirred at room temperature over night. The solvent was removed by evaporation under reduced pressure and the crude reaction mixture extracted from a saturated aqueous solution of sodium bicarbonate (100 mL) with ethyl acetate (three times 100 mL). The combined organic phases were dried over sodium sulfate and purified by silica gel column chromatography using a MPLC system (CombiFlash Companion, Isco Inc.) eluting with a gradient of n-heptane:ethyl acetate to give 4.2 g (49%) of the title compound as a light yellow solid. MS (ISP): m/z=175.4 [M+H]+.

後処理

  1. customThe solvent was removed by evaporation under reduced pressure
  2. customthe crude reaction mixture
  3. extractionextracted from a saturated aqueous solution of sodium bicarbonate (100 mL) with ethyl acetate (three times 100 mL)
  4. dry with materialThe combined organic phases were dried over sodium sulfate
  5. custompurified by silica gel column chromatography
  6. washeluting with a gradient of n-heptane

出典と根拠

ORDレコード
ord-b0474f9d64ee40d68ed2fcead35349dd
出典データセット
uspto-grants-2014_05
特許番号
US08729091B2

関連ノート

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