Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Iodothiophene | HCID 18921 | — |
| 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 | Dichloromethane | HCID 6344 | — |
| Product | HCID 57557246 | HCID 57557246 | 19.8% |
Reaction Steps
Tris(dibenzylideneacetone)dipalladium(0) chloroform adduct (0.112 g, 0.03 eq.), 2-iodothiophene (3.9 g, 1.1 eq.), triethylamine (1.1 g, 3 eq.), and copper (I) iodide (0.042 g, 0.06 eq.) were added sequentially to a solution of 2-ethyl-1-(4-pentynyl)-1H-imidazo[4,5-c]quinolin-4-amine (1.0 g, 3.5 mmol, 1.0 eq.) in dichloromethane (20 mL). The reaction mixture was stirred at ambient temperature for 6 hours at which time analysis by liquid chromatography/mass spectroscopy indicated that the reaction was complete. The reaction mixture was absorbed onto the top of a column of silica gel (30 g) and the column was eluted sequentially with dichloromethane and 3/97 methanol/dichloromethane. The product was recrystallized from 1,2-dichloroethane to provide 0.25 g of 2-ethyl-1-[5-(thien-2-yl)-4-pentynyl]-1H-imidazo[4,5-c]quinolin-4-amine as an off white powder, mp 175.0-190.0° C. (dec.). 1H NMR (300 MHz, CDCl3) δ 8.09 (dd, J=8.3, 1.0 Hz, 1H), 7.82 (dd, J=8.3, 1.0 Hz, 1H), 7.48 (ddd, J=8.4, 6.9, 1.3 Hz, 1H), 7.24 (m, 3H), 6.99 (dd, J=5.1, 3.6 Hz, 1H), 5.37 (s, 2H), 4.65 (t, J=7.7 Hz, 2H), 3.01 (q, J=7.5 Hz, 2H), 2.63 (t, J=6.2 Hz, 2H), 2.23 (m, 2H), 1.49 (t, J=7.4 Hz, 3H); MS (APCI) m/z 361 (M+H)+; Anal. calcd for C21H20N4S.0.03C2H4Cl2: C, 69.88; H, 5.59; N, 15.51. Found: C, 69.59; H, 5.69; N, 15.34.
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-150e70ebf7764cdca323f2482fea1067 |
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| Source note | uspto-grants-2014_08 |
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