Hydrochloric Acid → 3-Chloro-4-((4-fluorotetrahydro-2h-pyran-4-yl)methoxy)benzenesulfonamide

HRID 624463ノート

反応式

HRID 624463 の反応式
[F:1][C:2]1([CH2:8][OH:9])[CH2:7][CH2:6][O:5][CH2:4][CH2:3]1.[H-].[Na+].[Cl:12][C:13]1[CH:14]=[C:15]([S:20]([NH2:23])(=[O:22])=[O:21])[CH:16]=[CH:17][C:18]=1F.Cl>O1CCCC1.ClCCl.CN(C)C=O>[Cl:12][C:13]1[CH:14]=[C:15]([S:20]([NH2:23])(=[O:21])=[O:22])[CH:16]=[CH:17][C:18]=1[O:9][CH2:8][C:2]1([F:1])[CH2:7][CH2:6][O:5][CH2:4][CH2:3]1

参加物

8

実験手順

To a solution of EXAMPLE 296C (0.175 g) in tetrahydrofuran (5 ml) was added sodium hydride (0.209 g) and the reaction stirred at room temperature for 15 minutes. 3-Chloro-4-fluorobenzenesulfonamide (0.273 g) was added and the reaction stirred for 3 hours. To the thick suspension was added tetrahydrofuran (2 ml) and N,N-dimethylformamide ml). The reaction was stirred for 3 hours at 60° C. then poured into dichloromethane (50 ml) and 1N aqueous HCl (50 ml). The organic layer was washed with brine (35 ml) dried over magnesium sulfate, filtered, and concentrated. Silica gel chromatography (Reveleris 40 g) eluting with a gradient of 10-100% ethyl acetate, hexanes over 30 minutes (flow=40 ml/minute) gave the title compound.

後処理

  1. stirringthe reaction stirred for 3 hours
  2. stirringThe reaction was stirred for 3 hours at 60° C.
  3. washThe organic layer was washed with brine (35 ml)
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. washSilica gel chromatography (Reveleris 40 g) eluting with a gradient of 10-100% ethyl acetate, hexanes over 30 minutes (flow=40 ml/minute)

出典と根拠

ORDレコード
ord-7db9e72e0bab438c8280eec200e2f639
出典データセット
uspto-grants-2016_04
特許番号
US09303025B2

反応ノート

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