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Hydrochloric Acid → 1-(4-Fluorophenyl)-1H-pyrazol-5-ylboronic acid

HRID 2202451
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HRID 2202451 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH:12]=[CH:11][CH:10]=[N:9]2)=[CH:4][CH:3]=1.[Li+].CCC[CH2-].[B:18](OC(C)C)([O:23]C(C)C)[O:19]C(C)C.Cl>C1COCC1>[F:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]2[C:12]([B:18]([OH:23])[OH:19])=[CH:11][CH:10]=[N:9]2)=[CH:6][CH:7]=1
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참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 21531Triisopropyl borateHCID 61028n-Butyl lithiumHCID 199371841-(4-fluorophenyl)-1H-pyrazole

생성물 1

HCID 900951701-(4-Fluorophenyl)-1H-pyrazol-5-ylboronic acid수율 24%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran
용매

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온도
-78 °C

실험 절차

To a stirred solution of commercially available 1-(4-fluorophenyl)-1H-pyrazole [CAS No 81329-32-0] (1.6 g, 9.87 mmol) in THF (39.5 ml) was added drop wise at −78° C. under nitrogen atmosphere N-butyllithium (1.6 N in hexane, 6.47 ml, 10.4 mmol). After the mixture was allowed to stir at −78° C. for 1 h triisopropyl borate (7.65 g, 9.35 ml, 39.5 mmol) was added at −78° C. The mixture was allowed to stir at −78° C. for 1 h, gradually warmed to room temperature, and the pH of the mixture was adjusted to 5 with 1 M HCl solution. The mixture was evaporated and the remaining water layer extracted with ethyl acetate (2×30 ml). The combined organic layers were washed with brine (30 ml), dried over MgSO4 and evaporated. The raw product was purified by column chromatography on silica gel (dichloromethane/MeOH) and trituration (diethyl ether/hexane) to yield the title compound as a white solid (479 mg, 24%), MS (ISN) m/z=205.0 [(M−H)−], mp 115° C.

후처리

  1. additionwas added at −78° C
  2. temperaturegradually warmed to room temperature
  3. customThe mixture was evaporated
  4. extractionthe remaining water layer extracted with ethyl acetate (2×30 ml)
  5. washThe combined organic layers were washed with brine (30 ml)
  6. dry with materialdried over MgSO4
  7. customevaporated
  8. customThe raw product was purified by column chromatography on silica gel (dichloromethane/MeOH) and trituration (diethyl ether/hexane)

출처 및 근거

ORD 기록
ord-a21aa21d000449bda4bfebfc4eba66c7
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09365550B2

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