Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | N-[5-(4,5-diphenyl-1H-imidazol-2-ylthio)pentyl]-heptanamine | HCID 10048624 | — |
| Reactant | HCID 19021736 | HCID 19021736 | — |
| Solvent | Diphenyl Ether | HCID 7583 | — |
| Product | HCID 86747907 | HCID 86747907 | — |
Reaction Steps
A mixture of N-[5-(4,5-diphenyl-1H-imidazol-2-ylthio)pentyl]-1-heptanamine (4.35 g; 0.01 mol) and pyridyltosylurea (3.2 g; 0.011 mol; Frigola Conatansa, Jordi; ES 534,782) in diphenyl ether (35 mLs) was stirred under nitrogen at 180° C. for 30 minutes. The cooled solution was chromatographed with 1:1 hexane:ethyl acetate to give the title compound (4.03 g; 0.0073 mol) as an orange oil. 1H NMR (CDCl3) δ 8.15-8.05(m, 1H), 7.9(d, 1H, J=8.4 Hz), 7.6-7.4(m, 5H), 7.3-7.1 (m, 8H), 6.9-6.8 (m, 1H), 3.32 (t, 2H, J=7.2 Hz), 3.25(t,2H, J=7.9 Hz), 3.05(t,2H, J=6.6 Hz), 1.8-1.45(m,8H), 1.4-1.2(m, 8H), 0.9(t,3H, J=6.8 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05318984 |
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| Source dataset | uspto-grants-1994_06 |
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| ORD ID | ord-2df9b240320f4e0fa5356a82eed3a934 |
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| Source note | uspto-grants-1994_06 |
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