HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → HCID 24958969, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | HCID 68492838 | HCID 68492838 | — |
| Reactant | HCID 68492935 | HCID 68492935 | — |
| Product | HCID 24958969 | HCID 24958969 | 11% |
Reaction Steps
Following the procedure as described in Example 18, making variations as necessary to replace 1-(5-(benzylcarbamoyl)-4-methylthiazol-2-yl)-1H-1,2,3-triazole-4-carboxylic acid with 1-(5-(benzylcarbamoyl)-4-methylthiazol-2-yl)-5-methyl-1H-1,2,3-triazole-4-carboxylic acid to react with benzylamine, the title compound was obtained as a white solid in 11% yield (0.033 g): mp 183-186° C. (methanol); 1H NMR (300 MHz, DMSO-d6) δ 9.30 (t, J=6.0 Hz, 1H), 9.01 (t, J=6.0 Hz, 1H), 7.36-7.22 (m, 10H), 4.46 (d, J=6.0 Hz, 4H), 2.90 (s, 3H), 2.64 (s, 3H); 13C NMR (75 MHz, DMSO-d6) δ 160.1, 159.9, 155.1, 152.4, 139.4, 139.2, 138.9, 137.5, 128.3, 128.2, 127.3, 127.2, 126.9, 126.7, 125.1, 42.8, 41.9, 17.2, 10.3; MS (ES+) m/z 447.4 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08258160B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-a1ba8eedf5544709a1d08349afb1096a |
| Source note | uspto-grants-2012_09 |