反応 #1138

ord-9501c188203f4630b6447cbfdf010c16

反応方程式

CC(C)(C)OC(=O)N1CCCC1c1cncc(Br)c1
5-bromo-3-(1-tert-butyloxycarbonyl-2-pyrrolidinyl)pyridine
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
O=C([O-])[O-].[K+].[K+]
potassium carbonate
C#CC(C)(C)O
2-methyl-3-butyn-2-ol
C#CC(C)(O)Cc1cncc(C2CCCN2C(=O)OC(C)(C)C)c1
5-(2-hydroxy-2-methyl-3-butynyl)-3-(1-tert-butyloxycarbonyl-2-pyrrolidinyl)pyridine
収率 76.4%

反応条件

温度
25°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度the reaction flask was heated at 80° C. for 18 h
  2. 2
    ろ過this was filtered through celite
  3. 3
    その他The organic phase was separated
  4. 4
    抽出the aqueous layer extracted with ethyl acetate (3×20 mL)
  5. 5
    洗浄the combined ethyl acetate extracts were washed with brine (20 mL)
  6. 6
    乾燥dried (MgSO4)
  7. 7
    濃縮concentrated in vacuo
  8. 8
    その他The crude product was purified by silica gel column chromatography with ethyl acetate:hexane (1:3 to 1:1) as eluants

実験手順

A mixture of 5-bromo-3-(1-tert-butyloxycarbonyl-2-pyrrolidinyl)pyridine (1 g, 3.06 mmol), 10% palladium on charcoal (80 mg, 0.077 mmol), copper(I)iodide (58 mg, 0.30 mmol), triphenylphosphine (80 mg, 0.30 mmol) and potassium carbonate (1.06 g, 7.65 mmol) in DME (5 mL) and water (5 mL) was stirred at 25° C. After 0.75 h 2-methyl-3-butyn-2-ol (0.74 mL, 7.65 mmol) was added and the reaction flask was heated at 80° C. for 18 h. Water (30 mL) and ethyl acetate (30 mL) were added to the cooled mixture and this was filtered through celite. The organic phase was separated and the aqueous layer extracted with ethyl acetate (3×20 mL) and the combined ethyl acetate extracts were washed with brine (20 mL), dried (MgSO4) and concentrated in vacuo. The crude product was purified by silica gel column chromatography with ethyl acetate:hexane (1:3 to 1:1) as eluants to afford 5-(2-hydroxy-2-methyl-3-butynyl)-3-(1-tert-butyloxycarbonyl-2-pyrrolidinyl)pyridine as an oil (772 mg, 76%). LRMS (EI) m/e 231 (M+ +H --CO2 and isobutylene), 230 (M+ --CO2 and isobutylene), 229 (M+ --CO2 tBu); 1H NMR (CDCl3, 300 MHz): δ 8.56 (b-s, 1H), 8.37 (b-d, J=1.5 Hz, 1H), 7.53 (m, 1H), 4.93 (b-m, 0.5H), 4.76 (b-m, 0.5H), 3.5-3.7 (b-m, 2H), 2.36 (m, 1H), 1.75-2.0 (b-m, 3H), 1.72 (b-s, 1H), 1.63 (s, 6H), 1.45 (b-s, 3H), 1.21 (b-s, 6H).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05723477uspto-grants-1998_03