Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Iodobenzene | HCID 11575 | — |
| Reactant | HCID 86626642 | HCID 86626642 | — |
| 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 69080726 | HCID 69080726 | 6.6% |
Reaction Steps
Tris(dibenzylideneacetone)dipalladium(0) chloroform adduct (62.1 mg, 0.03 eq.), 4-iodobenzene (0.45 g, 1.1 eq.), triethylamine (0.61 g, 3 eq.), and copper (1) iodide (23 mg, 0.06 eq.) were added sequentially to a solution of 2-ethyl-1-(2-propynyl)-1H-imidazo[4,5-c]quinolin-4-amine (0.5 g, 2.0 mmol, 1.0 eq) in DMF. The reaction mixture was stirred at ambient temperature overnight. The reaction mixture was concentrated under reduced pressure to provide crude product which was purified by column chromatography (silica gel eluting with 8/92 methanol/dichloromethane). The residue was purified by recrystallization from 1,2-dichloroethane to provide 60 mg of 2-ethyl-1-(3-phenyl-2-propynyl)-1H-imidazo[4,5-c]quinolin-4-amine hydroiodide as a brown powder, mp 200-212° C. (dec). 1H NMR (300 MHz, DMSO-d6) δ 13.25 (s, 1H), 8.79 (br, 2H), 8.53 (dd, J=0.9, 8.5 Hz, 1H), 7.86 (dd, J=0.9, 8.3 Hz, 1H), 7.74 (ddd, J=1.2, 7.2, 8.4 Hz, 1H), 7.66 (ddd, J=1.2, 7.2, 8.3 Hz, 1H), 7.36 (m, 5H), 5.82 (s, 2H), 3.15 (q, J=7.5 Hz, 2H), 1.43 (t, J=7.5 Hz, 3H); MS (APCI) m/z 327 (M+H)+; Anal. Calcd for C21H18N4.HI: C, 55.52; H, 4.22; N, 12.33. Found: C, 55.80; H, 3.94; N, 12.46.
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-8d78b3baea0a42dfb206b6a49bb25148 |
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| Source note | uspto-grants-2014_08 |
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