반응 #1483065

ord-3a3a7bf47a5a461b9817eb1e7e8b8f95

반응 방정식

COC(=O)c1ccc2cc[nH]c2c1
1H-indole-6-carboxylic acid methyl ester
BrCC1CCCCC1
cyclohexylmethyl bromide
[H-].[Na+]
sodium hydride
COC(=O)c1ccc2ccn(CC3CCCCC3)c2c1
1-cyclohexylmethyl-1H-indole-6-carboxylic acid methyl ester
수율 74.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척the organic layer was washed again with dilute NaHCO3 (25 mL)
  2. 2
    건조The organic layer was dried over Na2SO4
  3. 3
    여과filtered
  4. 4
    농축concentrated

실험 절차

To a solution of commercially available 1H-indole-6-carboxylic acid methyl ester (0.35 g, 2.0 mmol) and cyclohexylmethyl bromide (0.31 mL, 2.2 mmol) in DMF (2 mL) was added sodium hydride (92 mg, 2.3 mmol). After stirring at room temperature for 3 hr, the solution was diluted with water (25 mL) and ethyl acetate (75 mL), the organic layer was washed again with dilute NaHCO3 (25 mL) and then brine (25 mL). The organic layer was dried over Na2SO4, filtered and concentrated. The remaining residue was subjected to flash chromatography (ethyl acetate/hexane, 1:24) to provide 1-cyclohexylmethyl-1H-indole-6-carboxylic acid methyl ester as a white solid (0.40 g, 74% yield). 1H NMR (400 MHz, DMSO) δ 8.10 (s, 1H), 7.62 (m, 2W), 7.58 (d, 1H, J=3.1 Hz), 6.52 (d, 1H, J=3.1 Hz), 4.10 (d, 2H, J=7.4 Hz), 3.85 (s, 3H), 1.77 (m, 1H), 1.65-1.57 (m 3H), 1.46 (m, 2H), 1.19 (m, 3H), 0.98 (m, 2H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08900565B2uspto-grants-2014_12