2,3,5,6-Tetrafluorophenol → (S)-3-Benzyloxycarbonylamino-4-oxo-5-(2,3,5,6-tetrafluoro-phenoxy)-pentanoic Acid Tert-Butyl Ester

HRID 1432361

反応式

HRID 1432361 の反応式
[F-].[K+].[C:3]([O:7][C:8](=[O:26])[CH2:9][C@H:10]([NH:15][C:16]([O:18][CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)=[O:17])[C:11](=[O:14])[CH2:12]Br)([CH3:6])([CH3:5])[CH3:4].[F:27][C:28]1[C:33]([F:34])=[CH:32][C:31]([F:35])=[C:30]([F:36])[C:29]=1[OH:37]>CN(C=O)C>[C:3]([O:7][C:8](=[O:26])[CH2:9][C@H:10]([NH:15][C:16]([O:18][CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)=[O:17])[C:11](=[O:14])[CH2:12][O:37][C:29]1[C:30]([F:36])=[C:31]([F:35])[CH:32]=[C:33]([F:34])[C:28]=1[F:27])([CH3:6])([CH3:5])[CH3:4]

参加物

5

実験手順

Potassium fluoride (2.8 g), was added portionwise to a stirred solution of (S)-3-benzyloxycarbonylamino-5-bromo-4-oxo-pentanoic acid tert-butyl ester (18.6 g) and 2,3,5,6-tetrafluorophenol (9.3 g) in anhydrous DMF (250 mL) under nitrogen at room temperature. The mixture was then stirred for 18 hours before being quenched with ethyl acetate and water. The organic layer was removed and washed with sodium bicarbonate solution, dried (magnesium sulfate) and concentrated to give the sub-title product as an off-white solid (21.1 g, 96%); 1H NMR (400 MHz, CDCl3) δ 1.43 (9H, s), 2.76 (1H, dd), 3.06 (1H, dd), 4.67-4.71 (1H, m), 5.12 (1h, d), 5.22 (1H, d), 5.86 (1H, d), 7.35-7.38 (5H, m); 19F NMR (376 MHz, CDCl3) (proton decoupled) δ −13998, −140.00, −140.04, −140.06, −157.05, −157.07, −157.11, −157.13; MS ES (+) 486.23 (M+H).

後処理

  1. custombefore being quenched with ethyl acetate and water
  2. customThe organic layer was removed
  3. washwashed with sodium bicarbonate solution
  4. dry with materialdried (magnesium sulfate)
  5. concentrationconcentrated

出典と根拠

ORDレコード
ord-8584fd77fbce4f9db8f9b916463dacff
出典データセット
uspto-grants-2009_11
特許番号
US07612091B2

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