Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | 3-(1H-Indol-6-yl)-3-(1H-indol-3-yl)-propionic acid ethyl ester | HCID 59831664 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 59831665 | HCID 59831665 | — |
Reaction Steps
To a 0° C. suspension of MeNH2—HCl (97.9 mg, 1.45 mmol) in benzene (4 ml) was added Me3Al (2 M in toluene, 746 μl, 1.45 mmol). The mixture was stirred for 5 minutes and at room temperature for about 1.25 hours. A suspension of 3-(1H-indol-6-yl)-3-(1H-indol-3-yl)-propionic acid ethyl ester XXVII in benzene (15 ml) was added, and the resulting reaction mixture was stirred at reflux for 8 hours, and at room temperature for 16 hours. The reaction mixture was diluted with a saturated solution of NH4Cl (20 ml) and extracted with EtOAc. The organic layers were combined, dried over Na2SO4, filtered, concentrated, and purified via flash chromatography (DCM/MeOH) affording 3-(1H-Indol-6-yl)-3-(1H-indol-3-yl)-N-methyl-propionamide XXVIII as a yellow oil (86 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07803830B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-5f3018e52d6b4b158cf190492f82438c |
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| Source note | uspto-grants-2010_09 |
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