HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(2-Aminoethyl)piperidine → HCID 11546782, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(2-Aminoethyl)piperidine | HCID 33944 | — |
| Reactant | 5-(5-Ethyl-2-methyl-6-oxo-1,6-dihydropyridin-3-yl)thiophene-2-sulfonyl chloride | HCID 86610352 | — |
| Product | HCID 11546782 | HCID 11546782 | 60% |
Reaction Steps
5-(5-Ethyl-2-methyl-6-oxo-1,6-dihydropyridin-3-yl)thiophene-2-sulfonyl chloride is reacted with 2-(piperidin-1-yl)ethylamine as described in Steps 5 and 6, Example 24 to give the title compound as a white solid (60% yield). LC/MS: RT 2.07 min; m/e 410; 1H NMR (δ, ppm): 10.68 (1H, br), 8.39 (1H, s), 7.64 (1H, s), 7.35 (1H, s), 7.20 (1H, s), 3.25-3.50 (4H, m), 2.80-3.00 (2H, m), 2.10-2.60 (7H, m), 1.60-2.00 (4H, m), 1.20-1.40 (2H, m), 1.10 (3H, t).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08173682B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-368445e63b9d41a4a69196bf1da8cc2e |
| Source note | uspto-grants-2012_05 |