Ethyl bromoacetate → HCID 66636183, compound

HRID 641437Notes

Reaction equation

HRID 641437 reaction equation
[H-].[Na+].[CH:3]([C:6]1[NH:7][C:8]2[C:13]([C:14]=1[CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])=[C:12]([N+:21]([O-:23])=[O:22])[CH:11]=[CH:10][CH:9]=2)([CH3:5])[CH3:4].Br[CH2:25][C:26]([O:28][CH2:29][CH3:30])=[O:27]>CN(C=O)C>[CH:3]([C:6]1[N:7]([CH2:25][C:26]([O:28][CH2:29][CH3:30])=[O:27])[C:8]2[C:13]([C:14]=1[CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])=[C:12]([N+:21]([O-:23])=[O:22])[CH:11]=[CH:10][CH:9]=2)([CH3:4])[CH3:5]

Participants

5

Procedure

Sodium hydride (45 mg of a 60% dispersion in mineral oil, 1.13 mmol) was added to a solution of ethyl (2-isopropyl-4-nitro-1H-indol-3-yl)acetate from Step E (300 mg, 1.03 mmol) in DMF (10 mL). After 5 min, ethyl bromoacetate (0.126 mL, 1.13 mmol) was added dropwise and the reaction mixture was stirred at ambient temperature for 30 min. The reaction mixture was quenched with saturated aqueous NaHCO3 (10 mL) and extracted with CHCl3 (3×25 mL). The combined organic extracts were washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography, eluting with a gradient of CHCl3:MeOH—100:0 to 95:5, to give the title compound. MS: m/z=377 (M+1).

Workup

  1. customThe reaction mixture was quenched with saturated aqueous NaHCO3 (10 mL)
  2. extractionextracted with CHCl3 (3×25 mL)
  3. washThe combined organic extracts were washed with brine
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe crude product was purified by silica gel chromatography
  8. washeluting with a gradient of CHCl3

Sources & evidence

ORD record
ord-2ff8d4da748749afbd630699e9d567d8
Source dataset
uspto-grants-2010_04
Patent number
US07696192B2

Reaction notes

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