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Ethylmorpholine → (2R, 5E)-2-[(4S)-2,2-dimethyl-5-oxo-1,3-dioxolan-4-yl]-N-[(1S)-2,2-dimethyl-1-({[(1R)-1-phenylethyl]amino}carbonyl)propyl]-5-(3-fluoro-4-phenoxyphenyl)pent-4-enamide

HRID 1700987
ノート
印刷プレビュー

反応式

HRID 1700987 の反応式
CC1C=CC=CC=1P(C1C=CC=CC=1C)C1C=CC=CC=1C.[CH3:23][C:24]1([CH3:53])[O:28][C@@H:27]([C@@H:29]([CH2:49][CH:50]=[CH2:51])[C:30]([NH:32][C@H:33]([C:38]([NH:40][C@@H:41]([C:43]2[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=2)[CH3:42])=[O:39])[C:34]([CH3:37])([CH3:36])[CH3:35])=[O:31])[C:26](=[O:52])[O:25]1.Br[C:55]1[CH:60]=[CH:59][C:58]([O:61][C:62]2[CH:67]=[CH:66][CH:65]=[CH:64][CH:63]=2)=[C:57]([F:68])[CH:56]=1.C(N1CCOCC1)C>C(#N)C.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[CH3:53][C:24]1([CH3:23])[O:28][C@@H:27]([C@@H:29]([CH2:49]/[CH:50]=[CH:51]/[C:55]2[CH:60]=[CH:59][C:58]([O:61][C:62]3[CH:63]=[CH:64][CH:65]=[CH:66][CH:67]=3)=[C:57]([F:68])[CH:56]=2)[C:30]([NH:32][C@H:33]([C:38]([NH:40][C@@H:41]([C:43]2[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=2)[CH3:42])=[O:39])[C:34]([CH3:35])([CH3:36])[CH3:37])=[O:31])[C:26](=[O:52])[O:25]1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 7525EthylmorpholineHCID 80271Tri-o-tolylphosphineHCID 227363164-Bromo-2-fluoro-1-phenoxybenzeneHCID 57042918(2R)-2-[(4S)-2,2-dimethyl-5-oxo-1,3-dioxolan-4-yl]-N-[(1S)-2,2-dimethyl-1-({[(1R)-1-phenylethyl]amino}carbonyl)propyl]pent-4-enamide

生成物 1

HCID 59875800
(2R, 5E)-2-[(4S)-2,2-dimethyl-5-oxo-1,3-dioxolan-4-yl]-N-[(1S)-2,2-dimethyl-1-({[(1R)-1-phenylethyl]amino}carbonyl)propyl]-5-(3-fluoro-4-phenoxyphenyl)pent-4-enamide
収率 22.7%

試薬・触媒・溶媒 2

HCID 167845palladium(II) acetate触媒HCID 6342Acetonitrile溶媒2 回

実験手順

A mixture of palladium acetate (17 mg, 0.075 mmol) and tri-(2-methylphenyl)phosphine (46 mg, 0.15 mmol) in anhydrous acetonitrile (2 mL) was sonicated at room temperature for 1 min until a creamy-coloured suspension formed. This suspension was added via Pasteur pipette to a stirred solution of (2R)-2-[(4S)-2,2-dimethyl-5-oxo-1,3-dioxolan-4-yl]-N-[(1S)-2,2-dimethyl-1-({[(1R)-1-phenylethyl]amino}carbonyl)propyl]pent-4-enamide (650 mg, 1.5 mmol), 1-bromo-3-fluoro-4-phenoxybenzene (Preparation 10)(587 mg, 2.26 mmol), and N-ethylmorpholine (348 μL, 3.0 mmol) in anhydrous acetonitrile (2.5 mL) under nitrogen. The mixture was purged with nitrogen, then heated at reflux for 16 h. After being cooled, the mixture was poured into ethyl acetate (100 mL) and washed with 5% aqueous citric acid (30 mL), saturated aqueous sodium chloride (50 mL), dried (NaSO4), and concentrated under reduced pressure. The residue was purified by flash chromatography (gradient elution with dichloromethane:ether) to give mainly (2R, 5E)-2-[(4S)-2,2-dimethyl-5-oxo-1,3-dioxolan-4-yl]-N-[(1S)-2,2-dimethyl-1-({[(1R)-1-phenylethyl]amino}carbonyl)propyl]-5-(3-fluoro-4-phenoxyphenyl)pent-4-enamide as a pale yellow foam (210 mg, 22%). 1H nmr suggested that alkene isomers were also present. The mixture of alkenes was taken onto the next step (see b, below).

後処理

  1. customwas sonicated at room temperature for 1 min until a creamy-coloured suspension
  2. customformed
  3. customThe mixture was purged with nitrogen
  4. temperatureheated
  5. temperatureat reflux for 16 h
  6. temperatureAfter being cooled
  7. additionthe mixture was poured into ethyl acetate (100 mL)
  8. washwashed with 5% aqueous citric acid (30 mL), saturated aqueous sodium chloride (50 mL)
  9. dry with materialdried (NaSO4)
  10. concentrationconcentrated under reduced pressure
  11. customThe residue was purified by flash chromatography (gradient elution with dichloromethane:ether)

出典と根拠

ORDレコード
ord-a5347c3f957541cf8803a97585d0dca6
出典データセット
uspto-grants-2002_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06350907B1

反応ノート

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