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Phosphoric Acid → 4-(4-{[(Triisopropylsilyl)oxy]carbonyl}-1-piperazinyl)phenylboronic acid

HRID 1744063
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1744063
Br[C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH2:13][CH2:12][N:11]([C:14]([O:16][Si:17]([CH:24]([CH3:26])[CH3:25])([CH:21]([CH3:23])[CH3:22])[CH:18]([CH3:20])[CH3:19])=[O:15])[CH2:10][CH2:9]2)=[CH:4][CH:3]=1.C([O:30][B:31](OC(C)C)[O:32]C(C)C)(C)C.P(=O)(O)(O)O>C1(C)C=CC=CC=1.O1CCCC1>[CH:18]([Si:17]([CH:24]([CH3:26])[CH3:25])([CH:21]([CH3:23])[CH3:22])[O:16][C:14]([N:11]1[CH2:12][CH2:13][N:8]([C:5]2[CH:6]=[CH:7][C:2]([B:31]([OH:32])[OH:30])=[CH:3][CH:4]=2)[CH2:9][CH2:10]1)=[O:15])([CH3:20])[CH3:19]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 1004Phosphoric AcidHCID 21531Triisopropyl borateHCID 22235752Triisopropylsilyl 4-(4-bromophenyl)-1-piperazinecarboxylate

Produkt 1

HCID 222360254-(4-{[(Triisopropylsilyl)oxy]carbonyl}-1-piperazinyl)phenylboronic acid

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 1140TolueneLösungsmittel
HCID 8028
Tetrahydrofuran
Lösungsmittel

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

A solution of triisopropylsilyl 4-(4-bromophenyl)-1-piperazinecarboxylate (4.5 g, 10.2 mmoles) in toluene (17 mL) and tetrahydrofuran (17 mL) was degassed by bubbling nitrogen at room temperature via a fritted gas dispenser for 10 minutes and then cooled to −78° C. for the addition of butyllithium (4.9 mL as a 2.5 M solution in hexanes, 12.3 mmoles). The solution turned yellow and after 30 minutes, triisopropylborate (3 mL, 13.3 mmoles) was added and the solution was warmed to 0° C. over 2.5 h prior to quenching with sat. aq. ammonium chloride (22 mL). To the flask was added 0.825 mL of phosphoric acid (14.8 M, 12.3 mmoles). The solution was stirred for 30 minutes. The phases were separated and the organic phase was dried over sodium sulfate. Right after filtering off the drying agent, the organic phase was washed with wet tetrahydrofuran (approx 2% water). The solution was concentrated to approx 15 mL. While concentrating, three 0.5 mL-portions of water were added to prevent boroxine formation. At this point, hexane was added and the resulting precipitate was filtered to yield 4-(4-{[(triisopropylsilyl)oxy]carbonyl}-1-piperazinyl)phenylboronic acid.

Aufarbeitung

  1. customby bubbling nitrogen at room temperature via a fritted gas dispenser for 10 minutes
  2. temperaturethe solution was warmed to 0° C. over 2.5 h
  3. customto quenching with sat. aq. ammonium chloride (22 mL)
  4. customThe phases were separated
  5. dry with materialthe organic phase was dried over sodium sulfate
  6. filtrationRight after filtering off the drying agent
  7. washthe organic phase was washed with wet tetrahydrofuran (approx 2% water)
  8. concentrationThe solution was concentrated to approx 15 mL
  9. concentrationWhile concentrating
  10. additionthree 0.5 mL-portions of water were added
  11. additionAt this point, hexane was added
  12. filtrationthe resulting precipitate was filtered

Quellen und Nachweise

ORD-Eintrag
ord-d5e3906d5d3c4b17bafc9e4cbd4adba6
Quelldatensatz
uspto-grants-2006_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07012075B2

Notizen zur Reaktion

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