Water → 5-[Benzyl-(3-oxo-3,4-dihydro-2H-benzo[1,4]oxazine-6-sulfonyl)-amino]-2-fluoro-N-isopropyl-benzamide

HRID 1518997ノート

反応式

HRID 1518997 の反応式
[CH2:1]([NH:8][C:9]1[CH:10]=[CH:11][C:12]([F:21])=[C:13]([CH:20]=1)[C:14]([NH:16][CH:17]([CH3:19])[CH3:18])=[O:15])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N(C(C)C)CC)(C)C.[O:31]=[C:32]1[NH:37][C:36]2[CH:38]=[C:39]([S:42](Cl)(=[O:44])=[O:43])[CH:40]=[CH:41][C:35]=2[O:34][CH2:33]1.O>ClCCl>[CH2:1]([N:8]([S:42]([C:39]1[CH:40]=[CH:41][C:35]2[O:34][CH2:33][C:32](=[O:31])[NH:37][C:36]=2[CH:38]=1)(=[O:44])=[O:43])[C:9]1[CH:10]=[CH:11][C:12]([F:21])=[C:13]([CH:20]=1)[C:14]([NH:16][CH:17]([CH3:18])[CH3:19])=[O:15])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

参加物

6

実験手順

A solution of 5-benzylamino-2-fluoro-N-isopropyl-benzamide (30 mg, 0.1 mmol), diisopropylethylamine (37 μL, 0.2 mmol), and 3-oxo-3,4-dihydro-2H-1,4-benzooxazine-6-sulfonyl chloride (52 mg, 0.2 mmol) was refluxed in dry dichloromethane (3 ml) for 18 hrs. On cooling, water (10 ml) was added with stirring. The organic layer was separated, dried (PTFE frit), then concentrated in vacuo. The crude residue was purified by preparative TLC (10% v/v ethyl acetate/dichloromethane) to afford the title compound as an off white solid (23 mg). HPLC retention time 7.72 min. Mass spectrum (ES+) m/z 499 (M+H).

後処理

  1. temperatureOn cooling
  2. customThe organic layer was separated
  3. dry with materialdried (PTFE frit)
  4. concentrationconcentrated in vacuo
  5. customThe crude residue was purified by preparative TLC (10% v/v ethyl acetate/dichloromethane)

出典と根拠

ORDレコード
ord-c112b3bdc5b643b4a6f46c975aeb6790
出典データセット
uspto-grants-2015_07
特許番号
US09073834B2

反応ノート

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