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Potassium Carbonate → 4,6-Difluoro-5-(4-(1-hydroxycyclobutyl)phenyl)-1H-indole-3-carbaldehyde

HRID 1054574
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HRID 1054574 반응식
CC1(C)COB(B2OCC(C)(C)CO2)OC1.C([O-])(=O)C.[K+].Br[C:23]1[CH:28]=[CH:27][C:26]([C:29]2([OH:33])[CH2:32][CH2:31][CH2:30]2)=[CH:25][CH:24]=1.Br[C:35]1[C:36]([F:47])=[C:37]2[C:41](=[CH:42][C:43]=1[F:44])[NH:40][CH:39]=[C:38]2[CH:45]=[O:46].C(=O)([O-])[O-].[K+].[K+]>O1CCOCC1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2].CCO.C1(C)C=CC=CC=1>[F:47][C:36]1[C:35]([C:23]2[CH:28]=[CH:27][C:26]([C:29]3([OH:33])[CH2:32][CH2:31][CH2:30]3)=[CH:25][CH:24]=2)=[C:43]([F:44])[CH:42]=[C:41]2[C:37]=1[C:38]([CH:45]=[O:46])=[CH:39][NH:40]2
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참가 물질

10

반응물 5

HCID 11430Potassium CarbonateHCID 517044Potassium AcetateHCID 2734316Bis(neopentyl glycolato)diboronHCID 120954191-(4-Bromophenyl)cyclobutanolHCID 866985785-Bromo-4,6-difluoro-1H-indole-3-carbaldehyde

생성물 1

HCID 866985794,6-Difluoro-5-(4-(1-hydroxycyclobutyl)phenyl)-1H-indole-3-carbaldehyde
수율 66.5%

시약·촉매·용매 4

HCID 44119782Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)촉매2회HCID 702Ethanol용매HCID 1140Toluene용매HCID 312751,4-Dioxane용매

반응 조건

온도
110 °C

실험 절차

A mixture of 5,5,5′,5′-tetramethyl-2,2′-bi(1,3,2-dioxaborinane) (188.0 mg, 0.55 mmol), oven dried potassium acetate (230.0 mg, 2.34 mmol), and 1-(4-bromophenyl)cyclobutanol (114.0 mg, 0.50 mmol) in 1,4-dioxane (2 mL) was degassed with N2 for 15 min, then treated with [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (20.0 mg, 0.027 mmol). The reaction mixture was subjected to microwave irradiation at 110° C. for 1 hour. The cooled reaction mixture was filtered through celite, rinsed with EtOAc and concentrated to dryness. To the resulting dark solid ((45.0 mg, 0.17 mmol) was added 5-bromo-4,6-difluoro-1H-indole-3-carbaldehyde (45.0 mg, 0.17 mmol), 2 N aqueous potassium carbonate (0.20 mL, 0.40 mmol), toluene (1.5 mL) and EtOH (0.5 mL). The reaction mixture was degassed with N2 for 10 minutes, treated with [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (14.0 mg, 0.019 mmol), and heated in a sealed pressure tube at 110° C. for 2 hours. The reaction mixture was cooled to room temperature and purified by flash chromatography (0-67% EtOAc/heptanes) to give the title compound (37 mg, 65%) as a white solid. MS (ES+) 328.0 (M+H)+. 1H NMR (500 MHz, CD3OD) δ 10.04 (d, J=2.68 Hz, 1 H), 8.15 (s, 1 H), 7.64 (d, J=8.05 Hz, 2 H), 7.48 (d, J=8.05 Hz, 2 H), 7.21 (d, J=9.51 Hz, 1 H), 2.57-2.66 (m, 2 H), 2.39-2.46 (m, 2 H), 2.03-2.12 (m, 1 H), 1.73-1.83 (m, 1 H).

후처리

  1. customwas degassed with N2 for 15 min
  2. customirradiation at 110° C. for 1 hour
  3. customThe cooled reaction mixture
  4. filtrationwas filtered through celite
  5. washrinsed with EtOAc
  6. concentrationconcentrated to dryness
  7. customThe reaction mixture was degassed with N2 for 10 minutes
  8. temperatureThe reaction mixture was cooled to room temperature
  9. custompurified by flash chromatography (0-67% EtOAc/heptanes)

출처 및 근거

ORD 기록
ord-1f851abb00684c958da9bba46a587d7f
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09394285B2

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