HuagongsheHuagongshe Chemistry Print Report · For research reference only
[(5-Methyl-1,3,4-oxadiazol-2-yl)methyl]amine → HCID 46862361, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | [(5-Methyl-1,3,4-oxadiazol-2-yl)methyl]amine | HCID 14442192 | — |
| Reactant | (S)-N-(1-(2-cyanoethylamino)-3,3-dimethyl-1-oxobutan-2-yl)-3-(3,4-difluorophenyl)-6,7-dihydropyrano[4,3-c]pyrazole-1(4H)-carboxamide | HCID 46862252 | — |
| Product | HCID 46862361 | HCID 46862361 | — |
Reaction Steps
Compound 113 was prepared by the procedure described for the synthesis of compound 104 by replacing 2-cyanoethylamine with 2-aminomethyl-5-methyl-1,3,4-oxadiazole. LCMS (+ESI) m/z=489.3 [M+H]+. 1H NMR (CDCl3) δ 7.90 (d, J=9.3 Hz, 1H), 7.46-7.52 (m, 1H), 7.28-7.32 (m, 1H), 7.19-7.26 (m, 1H), 6.91 (br, 1H), 4.82 (s, 2H), 4.74-4.79 (m, 1H), 4.58-4.63 (m, 1H), 4.28 (d, J=9.3 Hz, 1H), 3.94 (t, J=5.6 Hz, 2H), 3.17 (br, 2H), 2.51 (s, 3H), 1.12 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08653127B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-ec382a75eeda42c0ad76bf26f53cc37f |
| Source note | uspto-grants-2014_02 |