Diisopropylethylamine → HCID 57743052, Verbindung

HRID 2043690Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2043690
O[CH:2]1O[C:5](=[O:7])[CH2:4][CH:3]1[CH2:8][CH2:9][CH3:10].CCN(C(C)C)C(C)C.Cl.[O:21]1[CH:25]=[C:24]([CH2:26][NH2:27])[CH:23]=[N:22]1>ClCCCl.CC(O)=O>[O:21]1[CH:25]=[C:24]([CH2:26][N:27]2[CH2:2][CH:3]([CH2:8][CH2:9][CH3:10])[CH2:4][C:5]2=[O:7])[CH:23]=[N:22]1

Komponenten

6

Versuchsvorschrift

A solution of 5-hydroxy-4-propyldihydrofuran-2(3H)-one x252 (0.44 g, 3.0 mmol) in dry DCE (8 ml), DIEA (0.364 g, 2.8 mmol), and several drops AcOH is added to a suspension of 1-isoxazol-4-ylmethanamine hydrochloride x251 (0.46 g, 3.0 mmol) in dry DCE, and NaHB(OAc)3 (0.976 g, 2.3 mmol) is added in 50 min. The reaction mixture is stirred at room temperature for 72 h and washed with 20% K2CO3 (2×25 ml). The aqueous layer is subjected to extraction with dichloromethane (3×30 ml). The combined organic layers are washed with brine (40 ml), dried over Na2SO4, and evaporated. The residue (0.55 g) is purified by chromatography on silicagel (chloroform/ethyl acetate 1/1) to afford 0.202 g of 1-(isoxazol-4-ylmethyl)-4-propylpyrrolidin-2-one 157 (yield 0.202 g, 32%).

Aufarbeitung

  1. additionis added in 50 min
  2. washwashed with 20% K2CO3 (2×25 ml)
  3. extractionThe aqueous layer is subjected to extraction with dichloromethane (3×30 ml)
  4. washThe combined organic layers are washed with brine (40 ml)
  5. dry with materialdried over Na2SO4
  6. customevaporated
  7. customThe residue (0.55 g) is purified by chromatography on silicagel (chloroform/ethyl acetate 1/1)

Quellen und Nachweise

ORD-Eintrag
ord-28b079f3fb3b455ea905b78765a71d86
Quelldatensatz
uspto-grants-2013_11
Patentnummer
US08586623B2

Notizen zur Reaktion

Wird geladen…