4-Penten-1-OL → HCID 86647499, Verbindung

HRID 389177

Reaktionsgleichung

Reaktionsgleichung von HRID 389177
[CH2:1]([OH:6])[CH2:2][CH2:3][CH:4]=[CH2:5].CCN(C(C)C)C(C)C.Cl[C:17](Cl)([O:19]C(=O)OC(Cl)(Cl)Cl)Cl.[NH2:28][C@@H:29]([CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH:40]=[CH2:41])[C:30]([O:32][CH2:33][CH3:34])=[O:31].[OH-].[Na+]>O1CCOCC1>[CH2:1]([O:6][C:17]([NH:28][C@@H:29]([CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH:40]=[CH2:41])[C:30]([O:32][CH2:33][CH3:34])=[O:31])=[O:19])[CH2:2][CH2:3][CH:4]=[CH2:5]

Komponenten

7

Versuchsvorschrift

To a stirred solution of pent-4-en-1-ol (0.62 g, 7.21 mmol) and DIPEA (1.26 mL, 7.21 mmol) in anhydrous 1,4-dioxane (20 ml), at 10° C. and under nitrogen, was slowly added a solution of triphosgene (0.75 g, 2.52 mmol) in anhydrous 1,4-dioxane (20 mL). The reaction mixture was stirred at RT for 1 hour, and ethyl (2S)-2-aminonon-8-enoate*HCl (0.85 g, 3.61 mmol) and 1 M aqueous NaOH (7.21 ml, 7.21 mmol) added, and the reaction mixture was heated to 50° C. for 15 hours. After cooling to RT, the reaction mixture was basified to pH 8 with 1M aqueous NaOH and extracted with ether (3×200 ml). The combined organic phases were washed with water (100 mL), brine (50 mL), dried over Na2SO4, filtered and concentrated. The residue was chromatographed on silica gel (5 to 75% EtOAc in hexane) to give the title compound (0.96 g). LRMS (ESI) m/z 312.5 [(M+H)+; calcd for C17H30NO4: 312.2].

Aufarbeitung

  1. temperaturethe reaction mixture was heated to 50° C. for 15 hours
  2. temperatureAfter cooling to RT
  3. extractionextracted with ether (3×200 ml)
  4. washThe combined organic phases were washed with water (100 mL), brine (50 mL)
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe residue was chromatographed on silica gel (5 to 75% EtOAc in hexane)

Quellen und Nachweise

ORD-Eintrag
ord-9b3472f1b54542038d9f5857c636b3fe
Quelldatensatz
uspto-grants-2013_02
Patentnummer
US08377874B2

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