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[2-(3-Chloro-2-fluoro-phenyl)-ethylamine]-carbamic methyl ester → 6-Chloro-5-fluoro-3,4-dihydroisoquinolin-1(2H)-one

HRID 2277580
ノート
印刷プレビュー

反応式

HRID 2277580 の反応式
C[O:2][C:3](=O)[NH2:4].[Cl:6][C:7]1[C:8]([F:16])=[C:9]([CH2:13][CH2:14]N)[CH:10]=[CH:11][CH:12]=1>O>[Cl:6][C:7]1[C:8]([F:16])=[C:9]2[C:10](=[CH:11][CH:12]=1)[C:3](=[O:2])[NH:4][CH2:14][CH2:13]2
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 86685919[2-(3-Chloro-2-fluoro-phenyl)-ethylamine]-carbamic methyl ester

生成物 1

HCID 717439956-Chloro-5-fluoro-3,4-dihydroisoquinolin-1(2H)-one収率 4%

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
150 °C

実験手順

[2-(3-Chloro-2-fluoro-phenyl)-ethylamine]-carbamic methyl ester (890 mg, 3.85 mmol) and polyphosphoric acid (15 mL) were added to a 1-L, round bottom flask equipped with a magnetic stirring bar and reflux condenser. The reaction mixture was heated in an oil bath at 140-160° C. for 2 hours while keeping vigorous stirring. The reaction mixture was then allowed to cool to room temperature and poured into H2O (100 mL). After extraction with EtOAc, the organic layer was washed with brine, dried over anhy. MgSO4, filtered and concentrated to give a yellowish oil which was crystallized from Et2O to give title compound as a white solid (30 mg, 4%). MS: 200.1 (M+H)+.

後処理

  1. customequipped with a magnetic stirring bar
  2. temperaturereflux condenser
  3. temperatureto cool to room temperature
  4. extractionAfter extraction with EtOAc
  5. washthe organic layer was washed with brine
  6. customdried over anhy
  7. filtrationMgSO4, filtered
  8. concentrationconcentrated
  9. customto give a yellowish oil which
  10. customwas crystallized from Et2O

出典と根拠

ORDレコード
ord-827541a1ba7c45f199c1eb2fe3b7e4a2
出典データセット
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09133158B2

反応ノート

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