Tributylborane → 4-[2(4-Fluorophenyl)-4,4-dimethylcyclopenten-1-yl)benzenesulfonamide

HRID 1901105ノート

反応式

HRID 1901105 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH2:12][C:11]([CH3:14])([CH3:13])[CH2:10][C:9]=2[C:15]2[CH:20]=[CH:19][C:18]([S:21](C)(=[O:23])=[O:22])=[CH:17][CH:16]=2)=[CH:4][CH:3]=1.C(B(CCCC)CCCC)CCC.C([O-])(=O)C.[Na+].O[NH:44]S(O)(=O)=O>C1COCC1.C([Li])CCC.O>[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH2:12][C:11]([CH3:14])([CH3:13])[CH2:10][C:9]=2[C:15]2[CH:20]=[CH:19][C:18]([S:21]([NH2:44])(=[O:23])=[O:22])=[CH:17][CH:16]=2)=[CH:4][CH:3]=1

参加物

8

反応物 4

HCID 31216TributylboraneHCID 170246Hydroxysulfamic acidHCID 517045Sodium AcetateHCID 98410791-[2-(4-Fluorophenyl)-4,4-dimethyl-1-cyclopentenyl]-4-methylsulfonylbenzene

生成物 1

HCID 102690884-[2(4-Fluorophenyl)-4,4-dimethylcyclopenten-1-yl)benzenesulfonamide収率 43.9%

試薬・触媒・溶媒 3

HCID 178418339Butyllithium触媒HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

Under nitrogen, a solution of 4.55 g (13.2 mmol) of 1-[2-(4-fluoro phenyl)-4,4-dimethylcyclopenten-1-yl]-4-(methylsulfonyl)benzene (from Step 10 of Example 1) in 50 mL of THF at -78° C. was treated with 6.3 mL (0.27 mmol) of n-butyllithium (2.5M in hexane) over a period of 5 minutes. The reaction was stirred at ambient temperature for 25 minutes, cooled to -78° C., and treated with 19.8 mL (19.8 mmol ) of tributylborane (1.0M in THF). The resulting dark brown solution was stirred at ambient temperature for 30 minutes and then at reflux for 14 hours prior to the addition of 8.7 g (106 mmol) of sodium acetate, 37 mL of water, and 5.2 g (46 mmol) of hydroxyamine-O-sulfonic acid. The resulting light orange mixture was stirred at ambient temperature for 6 hours and the aqueous phase extracted with ethyl acetate. The combined extracts were washed with water, brine, dried (MgSO4), and concentrated in vacuo. The residue was chromatographed on silica gel to give 2.0 g (40%) of 4-[2(4-fluorophenyl)-4,4-dimethylcyclopenten-1-yl)benzenesulfonamide as a colorless solid: mp 117°-118° C.; NMR (CDCl3) δ1.24 (s, 6H), 2.70 (s, 4H), 4.72 (s, 2H), 6.92 (t, J=9 Hz, 2H), 7.09 (dd, J=9 and 7 Hz, 2H), 7.26 (d, J=8 Hz, 2H), 7.74 (d, J=9 Hz, 2H). HRMS. Calc'd for C19H20FNO2S: 345.1199. Found: 345.1194. Anal. Calc'd for [C19H20FNO2S+0.27 H2O]: C, 65.14; H, 5.91; N, 4.00; S, 9.11. Found: C, 65.07; H, 5.94; N, 3.86; S, 9.29.

後処理

  1. temperaturecooled to -78° C.
  2. stirringThe resulting dark brown solution was stirred at ambient temperature for 30 minutes
  3. temperatureat reflux for 14 hours
  4. stirringThe resulting light orange mixture was stirred at ambient temperature for 6 hours
  5. extractionthe aqueous phase extracted with ethyl acetate
  6. washThe combined extracts were washed with water, brine
  7. dry with materialdried (MgSO4)
  8. concentrationconcentrated in vacuo
  9. customThe residue was chromatographed on silica gel

出典と根拠

ORDレコード
ord-dcde1b72b33b469e8079b2fa89e2a8d1
出典データセット
uspto-grants-1996_11
特許番号
US05576339

反応ノート

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