反応 #1483064

ord-f89e4aa913364b80a1682c35f5efeb5f

反応方程式

O=C(O)c1ccc2[nH]ccc2c1
1H-indole-5-carboxylic acid
[H-].[Na+]
sodium hydride
CI
iodomethane
CN(C)C=O
DMF
COC(=O)c1ccc2c(ccn2C)c1
1-methyl-1H-indole-5-carboxylic acid methyl ester
収率 93.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The reaction mixture was then quenched with water (5 mL)
  2. 2
    workup.ADDITIONdiluted with ether (150 mL) and ethyl acetate (50 mL)
  3. 3
    洗浄After washing with aq. NH4Cl (100 mL), water (100 mL)
  4. 4
    乾燥brine (100 mL), the organic layer was dried over MgSO4
  5. 5
    ろ過filtered
  6. 6
    濃縮concentrated

実験手順

A solution of 1H-indole-5-carboxylic acid (1.6 g, 10 mmol), sodium hydride (1.2 g, 30 mmol), iodomethane (6.2 mL, 100 mmol) and DMF (40 mL) was stirred and room temperature for 24 hr. The reaction mixture was then quenched with water (5 mL) and diluted with ether (150 mL) and ethyl acetate (50 mL). After washing with aq. NH4Cl (100 mL), water (100 mL) and then brine (100 mL), the organic layer was dried over MgSO4, filtered and concentrated. The remaining material was subjected to flash chromatography (ethyl acetate/hexane 1:4) to provide 1-methyl-1H-indole-5-carboxylic acid methyl ester as a crystalline solid (1.77 g, 93% yield). 1H NMR (400 MHz, CDCl3) δ 8.40 (s, 1H), 7.94 (d, 1H, J=9.0 Hz), 7.34 (d, 1H, J=9.0 Hz), 7.12 (d, 1H, J=2.9 Hz), 6.60 (d, 1H, J=2.9 Hz), 3.94 (s, 3H), 3.83 (s, 3H).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08900565B2uspto-grants-2014_12