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Potassium Carbonate → HCID 57557431, 화합물

HRID 1522836
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HRID 1522836 반응식
Br[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([O:12][CH3:13])[CH:10]=2)[C:5](=[O:14])[N:4]([C:15]2[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=2)[CH:3]=1.C(=O)([O-])[O-].[K+].[K+].[C:29]1(B(O)O)[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1>C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[CH3:13][O:12][C:9]1[CH:10]=[C:11]2[C:6](=[CH:7][CH:8]=1)[C:5](=[O:14])[N:4]([C:15]1[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=1)[CH:3]=[C:2]2[C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 66827Phenylboronic AcidHCID 24962933HCID 24962933, 화합물

생성물 1

HCID 57557431HCID 57557431, 화합물수율 98%

시약·촉매·용매 1

HCID 178418397HCID 178418397, 화합물촉매

실험 절차

4-Bromo-6-methoxy-2-(4-methoxyphenyl)-isoquinolin-1(2H)-one (0.52 g, 1.44 mmol), tetrakis(triphenylphosphine)palladium (83 mg, 0.07 mmol), potassium carbonate (0.22 g, 1.00 mmol) and phenylboronic acid (0.21 g, 1.73 mmol) were placed in a dry and argon flushed 150 mL three-necked round-bottomed flask fitted with a stirring bar and reflux condenser. 1,2-Dimethoxyethane (10 mL) and water (3 mL) were added via a syringe under argon atmosphere. The reaction solution was stirred and heated to reflux for 20 hours. The reaction was quenched by adding 30 mL of water at room temperature. The mixture was extracted with ethyl acetate (3×20 mL). The extracts were combined, washed with brine (2×10 mL) and dried over anhydrous MgSO4 and 2 g of 3-(diethylenetriamino)propylfunctionalized silica gel followed by filtration and concentration to give a yellow residue. The yellow residue was purified by flash column chromatography (silica-gel, hexanes/ethyl acetate=2/3 v/v) to give a white solid product, 0.50 g, 98.0% yield. MS: m/z 358.3 [M+H]+. 1H NMR (DMSO-d6, 300 MHz) (8.30 (d, 2H, J=9.0 Hz), 7.55-7.40 (m, 8H), 7.29 (s, 1H), 7.21 (dd, 1H, J1=9.0 Hz, J2=2.4 Hz), 7.05 (d, 2H, J=9.0 Hz), 6.94 (d, 1H, J=2.4 Hz), 3.81 (s, 3H), 3.78 (s, 3H).

후처리

  1. customa dry
  2. customargon flushed 150 mL three-necked round-bottomed flask
  3. customfitted with a stirring bar
  4. temperaturereflux condenser
  5. addition1,2-Dimethoxyethane (10 mL) and water (3 mL) were added via a syringe under argon atmosphere
  6. temperatureheated
  7. temperatureto reflux for 20 hours
  8. customThe reaction was quenched
  9. additionby adding 30 mL of water at room temperature
  10. extractionThe mixture was extracted with ethyl acetate (3×20 mL)
  11. washwashed with brine (2×10 mL)
  12. dry with materialdried over anhydrous MgSO4 and 2 g of 3-(diethylenetriamino)propylfunctionalized silica gel
  13. filtrationfollowed by filtration and concentration
  14. customto give a yellow residue
  15. customThe yellow residue was purified by flash column chromatography (silica-gel, hexanes/ethyl acetate=2/3 v/v)
  16. customto give a white solid product, 0.50 g, 98.0% yield

출처 및 근거

ORD 기록
ord-959913a2a39243c3b97f37dd3d10a5c5
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09078888B2

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