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Water → 6-Fluoro-7-hydroxy-3,4-dihydroisoquinolin-1(2H)-one

HRID 1727402
ノート
印刷プレビュー

反応式

HRID 1727402 の反応式
[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][C:10]=1[OH:11])[C:7](=[O:12])[CH2:6][CH2:5]2.[N-:13]=[N+]=[N-].[Na+].O>C(Cl)(Cl)Cl>[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][C:10]=1[OH:11])[C:7](=[O:12])[NH:13][CH2:6][CH2:5]2
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 33557Sodium AzideHCID 448291085-Fluoro-6-hydroxy-2,3-dihydro-1H-inden-1-one

生成物 1

HCID 575676666-Fluoro-7-hydroxy-3,4-dihydroisoquinolin-1(2H)-one

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

To a solution of 5-fluoro-6-hydroxyindan-1-one ((90), 10.5 g, 63.3 mmol) in chloroform (600 ml) was added NaN3 (12.3 g, 190 mmol), followed by dropwise addition of methanasulfonic acid (33 ml, 506 mmol). Resulting mixture was stirred for 3 hr. The reaction mixture was poured into cold water and extracted with chloroform (3×). Organic extracts were combined and washed with H2O and sat. NaCl, then dried over Na2SO4. Concentration in vacuo gave a mixture of required product and reversed lactam. Purification of crude product on silica eluting with 30-60% EtOAc/Hexane offered the title compound as a off-white solid (5.3 g, 46%). MS (ES) m/z 180.0.

後処理

  1. customResulting mixture
  2. extractionextracted with chloroform (3×)
  3. washwashed with H2O and sat. NaCl
  4. dry with materialdried over Na2SO4
  5. concentrationConcentration in vacuo
  6. customgave

出典と根拠

ORDレコード
ord-4b662b4c53ca40ca9d9d63c668642cf3
出典データセット
uspto-grants-2009_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07495111B2

反応ノート

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