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Water → 8-Chloro-2,3-dihydro-1H-pyrido[2,3-B][1,4]oxazine

HRID 1943760
ノート
印刷プレビュー

反応式

HRID 1943760 の反応式
[Cl:1][C:2]1[C:11]2[NH:10][C:9](=O)[CH2:8][O:7][C:6]=2[N:5]=[CH:4][CH:3]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-].O.[OH-].[Na+]>O1CCCC1>[Cl:1][C:2]1[C:11]2[NH:10][CH2:9][CH2:8][O:7][C:6]=2[N:5]=[CH:4][CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962Water2 回HCID 14798Sodium HydroxideHCID 21226445Aluminium lithium hydrideHCID 669363978-Chloro-1H-pyrido[2,3-B][1,4]oxazin-2(3H)-one

生成物 1

HCID 669368298-Chloro-2,3-dihydro-1H-pyrido[2,3-B][1,4]oxazine

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran
溶媒
2 回

実験手順

8-chloro-1H-pyrido[2,3-b][1,4]oxazin-2-one (600 mg, 3.25 mmol) was dissolved in anhydrous tetrahydrofuran (16 ml) under nitrogen atmosphere, and then cooled to 0□. 1.0M Lithium aluminum hydride dissolved in tetrahydrofuran (6.5 ml, 6.50 mmol) was added thereto dropwise, and then stirred for 30 minutes. The reaction temperature was raised to room temperature and stirred for 1 hour. The reaction mixture was cooled to 0□ again, and water (0.26 ml), 10% sodium hydroxide solution (0.52 ml) and water (0.78 ml) were added thereto dropwise in this order, and then stirred vigorously at room temperature for 1 hour. The formed solid was filtered and washed with excess ethyl acetate.

後処理

  1. temperaturecooled to 0□
  2. additionwas added
  3. stirringstirred for 1 hour
  4. temperatureThe reaction mixture was cooled to 0□ again
  5. stirringdropwise in this order, and then stirred vigorously at room temperature for 1 hour
  6. filtrationThe formed solid was filtered
  7. washwashed with excess ethyl acetate

出典と根拠

ORDレコード
ord-ec825972028d462b9852b23d3056fc8d
出典データセット
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08394792B2

反応ノート

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