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Sodium Carbonate → 4-(5-fluoro-2-methoxyphenyl)-7-(phenylsulfonyl)-7H-pyrrolo[2,3-d]pyrimidine

HRID 527992
ノート
印刷プレビュー

反応式

HRID 527992 の反応式
Br[C:2]1[C:3]2[CH:10]=[CH:9][N:8]([S:11]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)(=[O:13])=[O:12])[C:4]=2[N:5]=[CH:6][N:7]=1.COCCOC.C(O)C.C(=O)([O-])[O-].[Na+].[Na+].[F:35][C:36]1[CH:37]=[CH:38][C:39]([O:45][CH3:46])=[C:40](B(O)O)[CH:41]=1>C(OCC)(=O)C>[F:35][C:36]1[CH:41]=[CH:40][C:39]([O:45][CH3:46])=[C:38]([C:2]2[C:3]3[CH:10]=[CH:9][N:8]([S:11]([C:14]4[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=4)(=[O:13])=[O:12])[C:4]=3[N:5]=[CH:6][N:7]=2)[CH:37]=1
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

6

反応物 4

HCID 10340Sodium CarbonateHCID 27826735-Fluoro-2-methoxyphenylboronic acidHCID 20074477Dimethoxyethane ethanolHCID 904185894-bromo-7-(phenylsulfonyl)-7H-pyrrolo[2,3-d]pyrimidine

生成物 1

HCID 904188734-(5-fluoro-2-methoxyphenyl)-7-(phenylsulfonyl)-7H-pyrrolo[2,3-d]pyrimidine

試薬・触媒・溶媒 1

HCID 8857
Ethyl Acetate
溶媒

反応条件

温度
100 °C

実験手順

To a suspension of Example 3A (5 g, 14.79 mmol) in 2:1 1,2-dimethyoxyethane/ethanol (150 mL) was added 2M aqueous sodium carbonate (29.6 mL, 59.1 mmol), (5-fluoro-2-methoxyphenyl)boronic acid (3.02 g, 17.74 mmol) and dichlorobis(triphenylphosphine) palladium(II) (1.038 g, 1.479 mmol). The mixture was heated at 100° C. for 1.5 hours, cooled and diluted with 100 mL ethyl acetate. The organic layer was washed with saturated sodium bicarbonate solution, water, and brine, dried over magnesium sulfate, filtered, and concentrated. The residue was triturated with dichloromethane, filtered, and dried under vacuum. The filtrate was concentrated to ⅓ volume, and the solid filtered and rinsed with dichloromethane. The remainder of the filtrate was purified by flash chromatography on silica (Analogix 280) eluting with a gradient of 15 to 70% ethyl acetate/hexane. This was combined with the triturated material and dried over vacuum to give the title compound. MS (ESI+) m/z 383.5 (M+H)+.

後処理

  1. temperaturecooled
  2. washThe organic layer was washed with saturated sodium bicarbonate solution, water, and brine
  3. dry with materialdried over magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe residue was triturated with dichloromethane
  7. filtrationfiltered
  8. customdried under vacuum
  9. concentrationThe filtrate was concentrated
  10. filtrationthe solid filtered
  11. washrinsed with dichloromethane
  12. customThe remainder of the filtrate was purified by flash chromatography on silica (Analogix 280)
  13. washeluting with a gradient of 15 to 70% ethyl acetate/hexane
  14. customdried over vacuum

出典と根拠

ORDレコード
ord-1eb5ce0404304813bd9c8a960f678188
出典データセット
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09346813B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート