Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromopropane | HCID 7840 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 10109086 | HCID 10109086 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 10309702 | HCID 10309702 | 82% |
Reaction Steps
To a solution of (±)-cis-2-(2,3-dichlorophenyl)-5,6,7a,8,9,10,11,11a-octahydro-4H-pyrido[3′,4′:4,5]pyrrolo[3,2,1-ij]quinoline (30 mg, 0.083 mmol) in 1,4-dioxane (0.5 mL) and N,N-diisopropylethylamine (108 mg, 0.83 mmol) were added 1-bromopropane (21 mg, 0.17 mmol) and KI (catalytic amount). The reaction mixture was heated at 100° C. for 15 h. The reaction mixture was cooled to 20° C. then concentrated in vacuo and chromatographed on a silica gel column by elution with CHCl3/MeOH (99/1) to give the title compound (27 mg, 82%) as a yellow oil. 1H NMR (CDCl3, 300 MHz) δ 0.92(t, J=7.3 Hz, 3H), 1.58–1.75 (br, 2H), 2.03–2.23 (m, 5H), 2.42–2.55 (br, 2H), 2.58–2.67 (m, 1H), 2.75 (t, J=7.4 Hz, 2H), 2.85–2.95 (br, 1H), 2.98–3.12 (br, 1H), 3.31 (dt, J=10.3, 3.6 Hz, 1H), 3.37–3.45 (br, 2H), 6.94 (s, 1H), 6.97 (s, 1H), 7.15–7.20 (m, 2H), 7.36–7.42 (m, 1H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07081455B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-8d1331317aa541ccb4ec4bba3244996b |
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| Source note | uspto-grants-2006_07 |
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