Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Ether hydrochloride | HCID 10953452 | — |
| Reactant | HCID 69497651 | HCID 69497651 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 11269280 | HCID 11269280 | — |
Reaction Steps
A solution of 3,4-dihydro-2H-pyrano[2,3-f]quinolin-3-amine (intermediate 1a) (0.20 g, 1.0 mmol), 3-(4-bromobutyl)-5-fluoro-1H-indole (0.19 g, 0.84 mmol), and triethylamine (0.28 mL, 1.68 mmol) in anhydrous dimethylsulfoxide (20 ml) was stirred at 100° C. for 14 hrs. The reaction mixture was poured into ice-H2O and extracted with methylene chloride. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under vacuum. Chromatography (5% MeOH/CH2Cl2) afforded 0.06 g (18%) of product as a light brown oil and unreacted starting material. It was converted to the HCl salt by dissolution in ethyl acetate and addition of 1M HCl/Et2O solution (2.4 eq) to generate N-[4-(5-fluoro-1H-indol-3-yl)butyl]-3,4-dihydro-2H-pyrano[2,3-f]quinolin-3-amine bis-hydrochloride salt as an off-white solid: mp 173° C./dec. MS ESI m/z 390 [M+H]+. Elemental Analysis for C24H24FN3O·2.00 HCl.3.00 H2O; Calculated: C, 55.82; H, 6.25; N, 8.14. Found: C, 55.57; H, 6.06; N, 7.76.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07227023B2 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-87f48d14cc7d432eb4f0da05996626a5 |
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| Source note | uspto-grants-2007_06 |
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