Hydrochloric Acid → HCID 86672697, compound
Reaction equation
C[O:2][CH:3](OC)[CH2:4][CH2:5][N:6]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][C:13]=2[C:15]([O:17][CH3:18])=[O:16])[CH:8]=[CH:7]1.Cl>C1COCC1>[O:2]=[CH:3][CH2:4][CH2:5][N:6]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][C:13]=2[C:15]([O:17][CH3:18])=[O:16])[CH:8]=[CH:7]1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of methyl 1-(3,3-dimethoxypropyl)-1H-indole-7-carboxylate (1.6 g, 5.8 mmol) from Step A above, 2 N HCl (15 mL) and THF (15 mL) were heated at reflux for 4 h. The reaction was quenched with solid sodium bicarbonate and adjusted to pH 8 and the aqueous phase was extracted with ethyl acetate (3×). The combined organics were washed with brine, dried over sodium sulfate, filtered, and concentrated under reduced pressure. The crude material was purified by column chromatography (silica gel, 80:20 hexanes/ethyl acetate) to give methyl 1-(3-oxopropyl)-1H-indole-7-carboxylate (278 mg, 21%) as a colorless oil: 1H NMR (500 MHz, CDCl3) δ 9.77 (s, 1H), 7.78 (d, J=8.0 Hz, 1H), 7.73 (d, J=7.5 Hz, 1H), 7.18 (d, J=3.0 Hz, 1H), 7.12 (t, J=8.0 Hz, 1H), 6.57 (d, J=3.0 Hz, 1H), 4.72 (t, J=6.5 Hz, 2H), 3.96 (s, 3H), 2.99 (t, J=6.5 Hz, 2H).
Workup
- temperatureat reflux for 4 h
- customThe reaction was quenched with solid sodium bicarbonate
- extractionthe aqueous phase was extracted with ethyl acetate (3×)
- washThe combined organics were washed with brine
- dry with materialdried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customThe crude material was purified by column chromatography (silica gel, 80:20 hexanes/ethyl acetate)
Sources & evidence
- ORD record
- ord-529fec96b57d42dda497bda2bc32f90d
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08710046B2
Reaction notes
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