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Sodium Carbonate → HCID 59631939, 화합물

HRID 2369035
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HRID 2369035 반응식
[CH3:1][O:2][C:3]([C:5]1[CH:9]=[C:8]([C:10]2[S:11][C:12](Br)=[CH:13][CH:14]=2)[N:7]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[Cl:22])[N:6]=1)=[O:4].[CH3:23][S:24]([C:27]1[CH:28]=[C:29](B(O)O)[CH:30]=[CH:31][CH:32]=1)(=[O:26])=[O:25].C(=O)([O-])[O-].[Na+].[Na+]>O1CCOCC1.O.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[Pd]>[CH3:1][O:2][C:3]([C:5]1[CH:9]=[C:8]([C:10]2[S:11][C:12]([C:31]3[CH:30]=[CH:29][CH:28]=[C:27]([S:24]([CH3:23])(=[O:26])=[O:25])[CH:32]=3)=[CH:13][CH:14]=2)[N:7]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[Cl:22])[N:6]=1)=[O:4]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 10340Sodium CarbonateHCID 27735423-(Methylsulfonyl)phenylboronic acidHCID 59633025HCID 59633025, 화합물

생성물 1

HCID 59631939HCID 59631939, 화합물수율 50.7%

시약·촉매·용매 3

HCID 11979704Tetrakis(triphenylphosphine)palladium촉매
HCID 962
Water
용매
HCID 312751,4-Dioxane용매

반응 조건

온도
90 °C

실험 절차

A mixture of 5-(5-bromo-thiophen-2-yl)-1-(2-chloro-phenyl)-1H-pyrazole-3-carboxylic acid methyl ester (8.0 g, 20 mmol), 3-methylsulfonylphenylboronic acid (5.0 g, 24 mmol), sodium carbonate (6.0 g, 56 mmol) and palladium tetrakis(triphenylphosphine) (1.2 g, 1.04 mmol) in 1,4-dioxane (100 mL) and H2O (5 mL) was stirred at 90° C. under N2 for 16 h. Solid was filtered off and washed with ethyl acetate. The filtrate was concentrated under vacuum to give a residue, which was partitioned between ethyl acetate and water. The aqueous layer was separated and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over sodium sulfate and evaporated to give a crude. It was triturated by DCM to afford 1-(2-chloro-phenyl)-5-[5-(3-methanesulfonyl-phenyl)-thiophen-2-yl]-1H-pyrazole-3-carboxylic acid methyl ester (4.8 g). The mother liquors from trituration were combined and concentrated to give a solid, which was purified by flash chromatography on silica gel eluted with EtOAc-hexane (0-60%) to afford another 2.8 g of product. The total yield was 7.6 g (80%). 1H-NMR (CDCl3): δ 8.04 (m, 1H), 7.84 (m, 1H), 7.73 (m, 1H), 7.50-7.58 (m, 4H), 7.47 (m, 1H), 7.23 (d, 1H), 7.20 (s, 1H), 6.82 (d, 1H), 3.98 (s, 3H), 3.07 (s, 3H).

후처리

  1. filtrationSolid was filtered off
  2. washwashed with ethyl acetate
  3. concentrationThe filtrate was concentrated under vacuum
  4. customto give a residue, which
  5. customwas partitioned between ethyl acetate and water
  6. customThe aqueous layer was separated
  7. extractionextracted with ethyl acetate
  8. washThe combined organic layers were washed with brine
  9. dry with materialdried over sodium sulfate
  10. customevaporated
  11. customto give a crude
  12. customIt was triturated by DCM

출처 및 근거

ORD 기록
ord-36452b1444ff43daa1b101162f2198a2
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08703805B2

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