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Hydrochloric Acid → 6-(Cyclopentyloxy)pyridine-3-boronic acid

HRID 646144
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HRID 646144 반응식
Br[C:2]1[CH:3]=[CH:4][C:5]([O:8][CH:9]2[CH2:13][CH2:12][CH2:11][CH2:10]2)=[N:6][CH:7]=1.[B:14](OC(C)C)([O:19]C(C)C)[O:15]C(C)C.[Li]CCCC.Cl>O.C1(C)C=CC=CC=1.C1COCC1>[CH:9]1([O:8][C:5]2[N:6]=[CH:7][C:2]([B:14]([OH:19])[OH:15])=[CH:3][CH:4]=2)[CH2:13][CH2:12][CH2:11][CH2:10]1
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참가 물질

8

반응물 4

HCID 313Hydrochloric AcidHCID 21531Triisopropyl borateHCID 219143535-Bromo-2-(cyclopentyloxy)pyridineHCID 178418339Butyllithium

생성물 1

HCID 574164386-(Cyclopentyloxy)pyridine-3-boronic acid수율 46.4%

시약·촉매·용매 3

HCID 962Water용매
HCID 1140
Toluene
용매
HCID 8028Tetrahydrofuran용매

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온도
-70 °C

실험 절차

To a mixture of 5-bromo-2-cyclopentoxypyridine (2.5 g, 10.3 mmol, see step (b) above), B(O-iPr)3 (2.33 g, 13.4 mmol), THF (4.1 mL) and toluene (16.5 mL) was portion-wise-added BuLi (2.5 M in hexane; 4.96 ml, 13.4 mmol) at −70° C. over 1 h. The reaction mixture was stirred over a further 40 min at −70° C. and then allowed to warm to −20° C. The acidity of the reaction mixture was adjusted to about pH 1 by addition of HCl (2 M aq. solution). The reaction was diluted with water (50 mL) and extracted with Et2O (2×50 mL). The pH of the water phase was then adjusted to about pH 7 by the addition of NaOH (5 M aq. solution). Brine was added and the product was extracted with EtOAc (4×50 mL). Removal of the solvent afforded the sub-title compound (0.99 g, 46%).

후처리

  1. temperatureto warm to −20° C
  2. extractionextracted with Et2O (2×50 mL)
  3. additionThe pH of the water phase was then adjusted to about pH 7 by the addition of NaOH (5 M aq. solution)
  4. additionBrine was added
  5. extractionthe product was extracted with EtOAc (4×50 mL)
  6. customRemoval of the solvent

출처 및 근거

ORD 기록
ord-1c42fefef91343c6a9611a03bff94a16
출처 데이터셋
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07705023B2

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