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'-(trifluoromethyl)biphenyl-4-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'-(trifluoromethyl)biphenyl-4-yl)-1,2,4-oxadiazole | HCID 66726712 | — |
| Product | 3-(Indolin-4-yl)-5-(2'-(trifluoromethyl)biphenyl-4-yl)-1,2,4-oxadiazole | HCID 66726733 | 99% |
Reaction Steps
When the product of Step C is 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 99% yield., as a colourless foam. 1H-NMR (CDCl3) 3.49 (tr, 2H, J=8.7 Hz); 3.66 (tr, 2H, J=8.7 Hz); 4.09 (broad s, 1H); 6.76 (d, 1H, J=7.6 Hz); 7.16 (tr, 1H, J=7.2 Hz); 7.34 (d, 1H, J=7.6 Hz); 7.4-7.63 (m, 5H); 7.77 (d, 1H, J=7.6 Hz); 8.24 (d, 1H, J=8.5 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09181182B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-dbb9f03fdb4a48b49d741340b9c3c3a7 |
| Source note | uspto-grants-2015_11 |