Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Chlorotriethylsilane | HCID 13819 | — |
| Reactant | HCID 86604024 | HCID 86604024 | — |
| Reactant | HCID 86604025 | HCID 86604025 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 21098845 | HCID 21098845 | 24.3% |
Reaction Steps
A solution of methyl (R)-(pyridin-3-yl)oxirane (1.17 g, 9.7 mmol) and methyl (R)-3-(2-aminopropyl)-1H-indole-7-carboxylate (1.50 g, 6.5 mmol) in methanol (10 mL) is stirred at 100° C. for 2 hours under sealed conditions, and the mixture is cooled and concentrated. The residue is dissolved in N,N-dimethylformamide (20 mL), and thereto are added imidazole (1.70 g, 25 mmol) and 4-dimethylaminopyridine (61 mg, 0.5 mmol) and triethylsilyl chloride (3.25 mL, 19.4 mmol). The mixture is stirred at room temperature for 3 hours, and thereto are added ethyl acetate. The mixture is washed with a saturated aqueous sodium hydrogen carbonate solution, water, and a saturated brine, dried over sodium sulfate, and concentrated. The residue is purified by silica gel column chromatography (methanol/chloroform=1/50) to give the desired methyl 3-[(2R)-2-(2-pyridin-3-yl-(2 R)-2-(triethylsilyloxy)ethyl-amino)propyl]-1H-indole-7-carboxylate (0.74 g, yield: 24%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07217724B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-d240c1cd55ab48808557f8daf31629be |
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| Source note | uspto-grants-2007_05 |
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