Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Iodoanisole | HCID 69676 | — |
| Reactant | HCID 86626645 | HCID 86626645 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | Palladium, tris[mu-[(1,2-eta:4,5-eta)-(1E,4E)-1,5-diphenyl-1,4-pentadien-3-one]]di-, compd. with trichloromethane (1:1) | HCID 11029508 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69080447 | HCID 69080447 | — |
Reaction Steps
Tris(dibenzylideneacetone)dipalladium(0) chloroform adduct (0.095 g, 0.03 eq.), 4-iodoanisole (0.786 g, 1.1 eq.), triethylamine (1.3 mL, 3 eq.), and copper (I) iodide (0.035 g, 0.06 eq.) were added sequentially to a solution of 2-ethyl-1-(4-pentynyl)-1H-imidazo[4,5-c]quinolin-4-amine (0.85 g, 3.0 mmol, 1.0 eq.) in DMF. The reaction mixture was stirred for about 4 hours and then concentrated under reduced pressure. The residue was purified by column chromatography (silica gel eluting with 4/96 methanol/dichloromethane) to provide an oil. The oil was recrystallized from ethanol to provide 2-ethyl-1-[5-(4-methoxyphenyl)-4-pentynyl]-1H-imidazo[4,5-c]quinolin-4-amine hydroiodide as off white granules, mp 230.0° C. 1H NMR (300 MHz, DMSO-d6) δ 13.14 (broad s, 1H), 8.65 (broad s, 2H), 8.37 (d, J=8.6 Hz, 1H), 7.83 (dd, J=8.4, 0.8 Hz, 1H), 7.68 (t, J=7.4 Hz, 1H), 7.41 (dt, J=8.1, 0.7 Hz, 1H), 7.34 (m, 2H), 6.93 (m, 2H), 4.73 (t, J=7.5 Hz, 2H), 3.77 (s, 3H), 3.08 (q, J=7.4 Hz, 2H), 2.66 (t, J=6.9 Hz, 2H), 2.09 (m, 2H), 1.41 (t, J=7.4 Hz, 3H); MS (APCI) m/z 385 (M+H)+; Anal. calcd for C24H24N4O1.HI.0.08C2H4Cl2: C, 55.30; H, 4.89; N, 10.69. Found: C, 55.39; H, 4.88; N, 10.63.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802853B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-84e5539e8c764158a937505fb1d4e27f |
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| Source note | uspto-grants-2014_08 |
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