HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Cyclopropylmethyl)piperidin-4-amine → 5-[5-Ethyl-2-methyl-6-oxo-1,6-dihydropyridin-3-yl]thiophene-2-sulfonic acid (1-cyclopropylmethylpiperidin-4-yl)amide hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Cyclopropylmethyl)piperidin-4-amine | HCID 17221624 | — |
| Reactant | 5-(5-Ethyl-2-methyl-6-oxo-1,6-dihydropyridin-3-yl)thiophene-2-sulfonyl chloride | HCID 86610352 | — |
| Product | 5-[5-Ethyl-2-methyl-6-oxo-1,6-dihydropyridin-3-yl]thiophene-2-sulfonic acid (1-cyclopropylmethylpiperidin-4-yl)amide hydrochloride | HCID 11698514 | 58% |
Reaction Steps
5-(5-Ethyl-2-methyl-6-oxo-1,6-dihydropyridin-3-yl)thiophene-2-sulfonyl chloride is reacted with (1-cyclopropylmethylpiperidin-4-yl)amine as described in Steps 5 and 6, Example 24 to give the title compound as a white solid (58% yield). LC/MS: RT 2.07 min; m/e 436; 1H NMR (δ, ppm): 11.85 (1H, br), 10.18 (1H, br), 8.30 (1H, d), 7.57 (1H, d), 7.34 (1H, s), 7.17 (1H, d), 3.30-3.58 (2H, m), 2.80-3.08 (2H, m), 2.40 (2H, q), 2.33 (3H, s), 1.72-2.18 (4H, m), 1.00-1.20 (4H, m), 0.60 (2H, m), 0.35 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08173682B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-0d5db943693a44ad8e5a26660b879428 |
| Source note | uspto-grants-2012_05 |