HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(1-Ethylpropyl)-6-methoxyisonicotinic acid → N-(2-Ethyl-4-{5-[2-(1-ethyl-propyl)-6-methoxy-pyridin-4-yl]-[1,2,4]oxadiazol-3-yl}-6-methyl-phenyl)-methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(1-Ethylpropyl)-6-methoxyisonicotinic acid | HCID 58418108 | — |
| Reactant | HCID 178436625 | HCID 178436625 | — |
| Product | N-(2-Ethyl-4-{5-[2-(1-ethyl-propyl)-6-methoxy-pyridin-4-yl]-[1,2,4]oxadiazol-3-yl}-6-methyl-phenyl)-methanesulfonamide | HCID 49872164 | 36.6% |
Reaction Steps
The title compound (24 mg) is prepared in analogy to Example 11 starting from 2-(1-ethyl-propyl)-6-methoxy-isonicotinic acid (32 mg, 143 μmol) and 3-ethyl-N-hydroxy-4-methanesulfonylamino-5-methyl-benzamidine (40 mg, 150 mmol); LC-MS**: tR=0.91 min, [M+H]+=459.09; 1H NMR (CDCl3): δ0.85 (t, J=7.3 Hz, 6H), 1.36 (t, J=7.3 Hz, 3H), 1.69-1.89 (m, 4H), 2.56 (s, 3H), 2.57-2.65 (m, 1H), 2.93 (q, J=7.5 Hz, 2H), 3.18 (s, 3H), 4.02 (s, 3H), 5.92 (s, 1H), 7.33 (s, 1H), 7.44 (s, 1H), 7.97 (s, 1H), 7.99 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08658675B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-ee34247045c842c499bb695179612d74 |
| Source note | uspto-grants-2014_02 |