Ethyl bromoacetate → HCID 66636183, compound
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
Reactant 3
Product 1
Reagents, catalysts & solvents 1
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
- customThe reaction mixture was quenched with saturated aqueous NaHCO3 (10 mL)
- extractionextracted with CHCl3 (3×25 mL)
- washThe combined organic extracts were washed with brine
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe crude product was purified by silica gel chromatography
- 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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