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

HRID 1744063
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HRID 1744063 반응식
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]
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참가 물질

6

반응물 3

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

생성물 1

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

시약·촉매·용매 2

HCID 1140Toluene용매
HCID 8028
Tetrahydrofuran
용매

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온도
-78 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-d5e3906d5d3c4b17bafc9e4cbd4adba6
출처 데이터셋
uspto-grants-2006_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07012075B2

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