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Water → HCID 86684921、化合物

HRID 2402904
ノート
印刷プレビュー

反応式

HRID 2402904 の反応式
Br[C:2]1[CH:7]=[CH:6][C:5]([S:8][CH2:9][CH2:10][C:11]([NH2:13])=[O:12])=[C:4]([C:14]([F:17])([F:16])[F:15])[CH:3]=1.C(=O)([O-])[O-].[K+].[K+].[CH3:24][C:25]1[CH:30]=[C:29](B2OC(C)(C)C(C)(C)O2)[CH:28]=[CH:27][N:26]=1.O>CN(C)C=O.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]>[CH3:24][C:25]1[CH:30]=[C:29]([C:2]2[CH:7]=[CH:6][C:5]([S:8][CH2:9][CH2:10][C:11]([NH2:13])=[O:12])=[C:4]([C:14]([F:17])([F:16])[F:15])[CH:3]=2)[CH:28]=[CH:27][N:26]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 962WaterHCID 11430Potassium CarbonateHCID 164142742-Methylpyridine-4-boronic acid pinacol esterHCID 86684910HCID 86684910、化合物

生成物 1

HCID 86684921HCID 86684921、化合物収率 74%

試薬・触媒・溶媒 2

HCID 44119782
Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)
触媒
HCID 6228Dimethylformamide溶媒

反応条件

温度
50 °C

実験手順

3-(4-Bromo-2-trifluoromethyl-phenylsulfanyl)-propionamide (300 g, 914 mmol) was dissolved in N,N-dimethylformamide (3.0 L) and potassium carbonate (300 g, 2.17 mol). Then, 2-methylpyridine-4-boronic acid pinacol ester (285 g, 1.3 mol) and water (240 mL) were added. The solution was degassed and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (30 g, 41 mmol) was added. The mixture was stirred for 20 h at 50° C. After cooling to room temperature, it was poured onto ice cold water (5° C., 5 L) and extracted with ethyl acetate (1×3.5 L, 2×1.5 L). The combined organic extracts were washed with brine/water (1:1 v/v, 750 mL) and brine (750 mL), before methanol (600 mL) was added and the mixture was dried over sodium sulfate. Silica gel (400 g) was added, the slurry was filtered and washed with ethyl acetate/methanol (9:1 v/v, 1.5 L). The combined filtrates were concentrated in vacuo. The residue was suspended in toluene (600 mL) and n-heptane (300 mL) and stirred for 5 min at 60° C. and for 1 h at room temperature. The precipitate was filtered off, washed with toluene/n-heptane (4:1 v/v, 300 mL) and n-heptane (300 mL), and dried in vacuo to afford 230.3 g of brown crystalline material. The crystals were further purified by trituration in isopropanol/heptane (1:1 v/v, 600 mL) for 30 min at room temperature and 30 min at 0-4° C. (ice bath). The precipitate was filtered off, washed with n-heptane/isopropanol (4:1 v/v, 300 mL), and dried in vacuo at 65° C. to yield the title compound as a light brown crystalline solid (215.7 g, 69%). MS (EI): m/z=341.1 [M+H]. 1H NMR (d6-DMSO, 400 MHz): δ 2.48 (t, J=7.2 Hz, 2H), 2.54 (s, 3H), 3.32 (t, J=7.2 Hz, 2H), 6.95 (bs, 1H), 7.41 (bs, 1H), 7.58 (dd, J=1.6 Hz, 5.4 Hz, 1H), 7.68 (s, 1H), 7.77 (d, J=9.1 Hz, 1H), 8.02-8.08 (m, 2H), 8.52 (d, J=5.1 Hz, 1H).

後処理

  1. customThe solution was degassed
  2. temperatureAfter cooling to room temperature
  3. additionit was poured onto ice cold water (5° C., 5 L)
  4. extractionextracted with ethyl acetate (1×3.5 L, 2×1.5 L)
  5. washThe combined organic extracts were washed with brine/water (1:1 v/v, 750 mL) and brine (750 mL), before methanol (600 mL)
  6. additionwas added
  7. dry with materialthe mixture was dried over sodium sulfate
  8. additionSilica gel (400 g) was added
  9. filtrationthe slurry was filtered
  10. washwashed with ethyl acetate/methanol (9:1 v/v, 1.5 L)
  11. concentrationThe combined filtrates were concentrated in vacuo
  12. stirringn-heptane (300 mL) and stirred for 5 min at 60° C. and for 1 h at room temperature
  13. filtrationThe precipitate was filtered off
  14. washwashed with toluene/n-heptane (4:1 v/v, 300 mL) and n-heptane (300 mL)
  15. customdried in vacuo

出典と根拠

ORDレコード
ord-1e70beceefc84de5b620c46b259ca9c2
出典データセット
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08796471B2

反応ノート

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