HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-(3,4-Diethoxyphenyl)-3-(1H-indol-4-yl)-1,2,4-oxadiazole → 3-(Indolin-4-yl)-5-(2-methylbenzofuran-5-yl)-1,2,4-oxadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-(3,4-Diethoxyphenyl)-3-(1H-indol-4-yl)-1,2,4-oxadiazole | HCID 25110297 | — |
| Reactant | 3-(1H-Indol-4-yl)-5-(2-methylbenzofuran-5-yl)-1,2,4-oxadiazole | HCID 66726607 | — |
| Product | 3-(Indolin-4-yl)-5-(2-methylbenzofuran-5-yl)-1,2,4-oxadiazole | HCID 66726611 | 100% |
Reaction Steps
When the product of Step D was substituted for 5-(3,4-diethoxyphenyl)-3-(1H-indol-4-yl)-1,2,4-oxadiazole in Example 34, Step C, the identical process afforded the title compound in 100% yield, as a colourless foam. 1H-NMR (CDCl3) 2.49 (s, 3H); 2.52 (broad s, 1H+H2O); 3.48 (tr, 2H, J=8.44 Hz); 3.68 (tr, 2H, J=8.44 Hz); 6.48 (s, 1H); 6.85 (d, 1H, J=7.75 Hz); 7.2 (tr, 2H, J=7.6 Hz); 7.38 (d, 1H, J=8.16 Hz); 7.51 (d, 1H, J=8.5 Hz); 8.06 (d, 1H, J=8.5 Hz); 8.32 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09181182B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-2c7bc2834b614b67991b3a9e9f03907c |
| Source note | uspto-grants-2015_11 |