Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 67217405 | HCID 67217405 | — |
| Reactant | HCID 67437256 | HCID 67437256 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 16202226 | HCID 16202226 | 251.9% |
Reaction Steps
A solution of [5-(3,4-dichloro-benzenesulfonyl)-8-fluoro-5,6-dihydro-phenanthridin-6-yl]-acetic acid (210 mg, 0.45 mmol), triethylamine (0.07 mL, 1.5 mmol) and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (0.19 g, 0.5 mmol) in dry dimethyl formamide (5 mL) was stirred at room temperature for five minutes before 2-[4-(4,5-dihydro-1H-imidazol-2-yl)-phenyl]-ethylamine dihydrochloride (Reference Example 2) (131 mg, 0.5 mmol) was added. The pH of the reaction mixture was adjusted to 8 by addition of triethylamine, the so obtained mixture was stirred at room temperature overnight, then concentrated in vacuo. The residue was purified by preparative thin-layer chromatography (dichloromethane:methanol:NH4OH=5:1:0.1) to yield 382 mg (75%) of the title compound as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08034827B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-a0aecb5ebc8e45ea93f644ea3ebe37ee |
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| Source note | uspto-grants-2011_10 |
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