HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pentylamine → HCID 11633885, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pentylamine | HCID 8060 | — |
| Reactant | 5-[4-(2-Trifluoromethylbenzoyl)piperazin-1-YL]-[1,3,4]thiadiazole-2-carboxylic acid ethyl ester | HCID 11582388 | — |
| Product | HCID 11633885 | HCID 11633885 | — |
Reaction Steps
Following the procedure as described in Example 3, making variations only as required to use n-pentylamine in place of isoamylamine to react with 5-[4-(2-trifluoromethylbenzoyl)piperazin-1-yl][1,3,4]thiadiazole-2-carboxylic acid ethyl ester, the title compound was obtained as a white solid (0.85 g, yield 77%). 1H NMR (300 MHz, CDCl3) δ 7.70-7.73 (m, 1H), 7.51-7.64 (m, 2H), 7.29-7.35 (m, 1H), 6.97-7.06 (m, 1H), 3.99-4.10 (m, 1H), 3.81-3.92 (m, 1H), 3.62-3.70 (m, 2H), 3.48-3.56 (m, 2H), 3.29-3.44 (m, 4H), 1.50-1.63 (m, 2H), 1.26-1.38 (m, 4H), 0.83-0.91 (m, 3H). 13C NMR (75 MHz, CDCl3) δ 174.6, 167.6, 158.3, 156.1, 133.1, 132.5, 129.7, 127.7, 126.9, 125.4, 121.8. MS (ES+) m/z 455.9 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07919496B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-df7830d0e6114e30affc75b15b65f6c7 |
| Source note | uspto-grants-2011_04 |