1-(Phenylmethyl) butanedioate → HCID 67133347、化合物

HRID 2421803ノート

反応式

HRID 2421803 の反応式
[CH2:1]([O:8][C:9](=[O:15])[CH2:10][CH2:11][C:12]([OH:14])=[O:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:16][C@@:17]12[C@H:25](O)[CH2:24][C@@H:20]([C:21]1([CH3:23])[CH3:22])[CH2:19][CH2:18]2.C1C=CC2N(O)N=NC=2C=1.CCN=C=NCCCN(C)C.Cl>CN(C1C=CN=CC=1)C.O1CCCC1>[C:9]([O:8][CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)(=[O:15])[CH2:10][CH2:11][C:12]([O:14][C@@H:18]1[CH2:19][C@H:20]2[C:21]([CH3:23])([CH3:22])[C@:17]1([CH3:16])[CH2:25][CH2:24]2)=[O:13]

参加物

7

反応条件

温度
50 °C

実験手順

In a 300 mL round bottom flask, fitted with reflux condenser, 4-(benzyloxy)-4-oxobutanoic acid (1.80 g, 1 eq., of Example 1) and anhydrous tetrahydrofuran (85 mL) were added. The reaction mixture was stirred under inert atmosphere and L-borneol (1.34 g, 1 eq.) was added, followed by the addition of HOBT (1.28 g, 1.1 eq.), EDC-HCl (1.81 g, 1.1 eq.) and DMAP (1.12 g, 1.1 eq). The reaction was heated in an oil bath at 50° C. for several hours until monitoring showed a substantial amount of product formation. The reaction mixture was filtered, concentrated and extracted with MTBE versus 1N HCl. The organic layer was washed with 1N HCl and brine, dried over MgSO4 and concentrated. The crude product was purified using column chromatography to give 1.83 g of a colorless oil (62%).

後処理

  1. customIn a 300 mL round bottom flask, fitted
  2. temperaturewith reflux condenser
  3. additionwas added
  4. filtrationThe reaction mixture was filtered
  5. concentrationconcentrated
  6. extractionextracted with MTBE versus 1N HCl
  7. washThe organic layer was washed with 1N HCl and brine
  8. dry with materialdried over MgSO4
  9. concentrationconcentrated
  10. customThe crude product was purified

出典と根拠

ORDレコード
ord-0386c5d6613848e5a775663732feb6c9
出典データセット
uspto-grants-2011_06
特許番号
US07959958B2

反応ノート

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