Sodium Carbonate → HCID 58032133, 화합물

HRID 1429238노트

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HRID 1429238 반응식
FC(F)(F)S(O[C:7]1[CH2:8][CH2:9][N:10]([C:13]2[C:18]([F:19])=[CH:17][C:16]([N+:20]([O-:22])=[O:21])=[CH:15][C:14]=2[F:23])[CH2:11][CH:12]=1)(=O)=O.[F:26][C:27]1[CH:28]=[C:29](B2OC(C)(C)C(C)(C)O2)[CH:30]=[CH:31][C:32]=1[F:33].[Cl-].[Li+].C(=O)([O-])[O-].[Na+].[Na+]>COCCOC.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>[F:19][C:18]1[CH:17]=[C:16]([N+:20]([O-:22])=[O:21])[CH:15]=[C:14]([F:23])[C:13]=1[N:10]1[CH2:11][CH:12]=[C:7]([C:30]2[CH:29]=[CH:28][C:27]([F:26])=[C:32]([F:33])[CH:31]=2)[CH2:8][CH2:9]1

참가 물질

7

반응물 4

HCID 10340Sodium CarbonateHCID 433294Lithium ChlorideHCID 534290432-(3,4-Difluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 58031995Methanesulfonic acid, 1,1,1-trifluoro-, 1-(2,6-difluoro-4-nitrophenyl)-1,2,3,6-tetrahydro-4-pyridinyl ester

생성물 1

HCID 58032133HCID 58032133, 화합물수율 63%

시약·촉매·용매 2

HCID 178418397HCID 178418397, 화합물촉매HCID 80711,2-Dimethoxyethane용매

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온도
100 °C

실험 절차

A mixture of 1-(2,6-difluoro-4-nitrophenyl)-1,2,3,6-tetrahydropyridin-4-yl trifluoromethanesulfonate (1.18 g, 3.04 mmol), 2-(3,4-difluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (1.02 g, 4.25 mmol), lithium chloride (0.387 g, 9.12 mmol) and a 2.0 M aq. solution of sodium carbonate (4.56 mL, 9.12 mmol) in anhydrous DME (15 mL) was vigorously stirred while bubbling with N2 gas for 20 minutes. Tetrakis(triphenylphosphine)palladium(0) (0.176 g, 0.152 mmol) was added, and the resulting mixture was degassed for 5 minutes more. The reaction flask was equipped with a condenser and placed in 100° C. oil bath. The dark mixture was stirred at 100° C. under a dry N2 atmosphere for 16 hours, and was then cooled to room temperature and partitioned between water (50 mL) and EtOAc (2×50 mL). The combined organic layers were dried over Na2SO4, filtered and concentrated in vacuo, and the crude product was purified by column chromatography on silica gel using a solvent gradient of 0-40% EtOAc in hexanes to provide a yellow oil that solidified on standing. The solid was triturated with Et2O and hexanes, filtered and dried to provide the title compound (0.67 g, 63%).

후처리

  1. customwhile bubbling with N2 gas for 20 minutes
  2. customthe resulting mixture was degassed for 5 minutes more
  3. customThe reaction flask was equipped with a condenser
  4. customplaced in 100° C.
  5. temperaturewas then cooled to room temperature
  6. custompartitioned between water (50 mL) and EtOAc (2×50 mL)
  7. dry with materialThe combined organic layers were dried over Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo
  10. customthe crude product was purified by column chromatography on silica gel using a solvent gradient of 0-40% EtOAc in hexanes
  11. customto provide a yellow oil that
  12. customThe solid was triturated with Et2O and hexanes
  13. filtrationfiltered
  14. customdried

출처 및 근거

ORD 기록
ord-3bcfcedad0834dec8dd9037c5bfee6a8
출처 데이터셋
uspto-grants-2015_01
특허 번호
US08937150B2

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