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Hydrochloric Acid → 4-[3-(4-Butyl-piperidin-1-yl)-propyl]-6-methyl-3,4-dihydro-2H-benzo[1,4]oxazine

HRID 969440
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 969440
B.[CH2:2]([CH:6]1[CH2:11][CH2:10][N:9]([CH2:12][CH2:13][CH2:14][N:15]2[C:20]3[CH:21]=[C:22]([CH3:25])[CH:23]=[CH:24][C:19]=3[O:18][CH2:17][C:16]2=O)[CH2:8][CH2:7]1)[CH2:3][CH2:4][CH3:5].Cl>C1COCC1>[CH2:2]([CH:6]1[CH2:7][CH2:8][N:9]([CH2:12][CH2:13][CH2:14][N:15]2[C:20]3[CH:21]=[C:22]([CH3:25])[CH:23]=[CH:24][C:19]=3[O:18][CH2:17][CH2:16]2)[CH2:10][CH2:11]1)[CH2:3][CH2:4][CH3:5]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 313Hydrochloric AcidHCID 6331BoraneHCID 102369054-[3-(4-Butyl-piperidin-1-yl)-propyl]-6-methyl-4H-benzo[1,4]oxazin-3-one

Produkt 1

HCID 101933994-[3-(4-Butyl-piperidin-1-yl)-propyl]-6-methyl-3,4-dihydro-2H-benzo[1,4]oxazine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Reaktionsbedingungen

Temperatur
40 °C

Versuchsvorschrift

A solution of borane in THF (1M, 0.5 mL, 0.5 mmol) was added to a solution of 4-[3-(4-butyl-piperidin-1-yl)-propyl]-6-methyl-4H-benzo[1,4]oxazin-3-one (50 mg, 0.15 mmol) in THF (6 mL). The reaction mixture was stirred at 40° C. for 16 h then aqueous HCl (4M, 10 mL) was added drop wise at room temperature. The reaction mixture was stirred for 16 h then concentrated in vacuo. A solution of K2CO3 (0.5 g) in water (5 mL) was added and the product was extracted with dichloromethane (2×10 mL). The organic layer was dried (Na2SO4) and concentrated in vacuo. The product was purified on an Isco CombiFlash Sq 16× (4 g silica column, eluting 0-20% ethyl acetate in heptanes+1% Et3N). Yield: 29.2 mg, 56%. HPLC-MS: M+1+=373.5 (UV/MS(%)=95/90). 1H NMR (400 MHz, CDCl3): δ=0.90 (3H, t), 1.18-1.35 (9H, m), 1.68 (2H, broad d), 1.78 (2H, quin.), 1.89 (2H, broad t), 2.24 (3H, s), 2.35 (2H, t), 2.89 (2H, broad d), 3.27 (2H, t), 3.31 (2H, t), 4.19 (2H, t), 6.39 (1H, broad d), 6.52 (1H, broad s), 6.66 (1H, d). 13C NMR (CDCl3): δ 14.3, 21.4, 23.1, 24.2, 29.3, 32.8 (2C), 36.1, 36.6, 47.4, 49.3, 54.5 (2C), 56.5, 64.7, 113.0, 116.2, 117.7, 131.1, 135.3, 142.0.

Aufarbeitung

  1. stirringThe reaction mixture was stirred for 16 h
  2. concentrationthen concentrated in vacuo
  3. additionA solution of K2CO3 (0.5 g) in water (5 mL) was added
  4. extractionthe product was extracted with dichloromethane (2×10 mL)
  5. dry with materialThe organic layer was dried (Na2SO4)
  6. concentrationconcentrated in vacuo
  7. customThe product was purified on an Isco CombiFlash Sq 16× (4 g silica column, eluting 0-20% ethyl acetate in heptanes+1% Et3N)

Quellen und Nachweise

ORD-Eintrag
ord-961d978390554af3b5f8fd88b176f1c2
Quelldatensatz
uspto-grants-2007_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07307075B2

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