HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-(aminomethyl)-N,N-dimethylpyridin-2-amine → 5-(5-Ethyl-2-methyl-6-oxo-1,6-dihydropyridin-3-yl)thiophene-2-sulfonic acid [(6-dimethylaminopyridin-3-yl)methyl]amide hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-(aminomethyl)-N,N-dimethylpyridin-2-amine | HCID 16788596 | — |
| 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 [(6-dimethylaminopyridin-3-yl)methyl]amide hydrochloride | HCID 11634161 | 55% |
Reaction Steps
5-(5-Ethyl-2-methyl-6-oxo-1,6-dihydropyridin-3-yl)thiophene-2-sulfonyl chloride is reacted with [(6-dimethylaminopyridin-3-yl)methyl]amine as described in Steps 5 and 6, Example 24 to give the title compound as a yellow solid (55% yield). LC/MS: RT 2.07 min; m/e 433; 1H NMR (δ, ppm): 11.86 (1H, br), 8.57 (1H, t), 7.80-7.95 (2H, m), 7.54 (1H, d), 7.43 (1H, s), 7.21 (1H, d), 7.14 (1H, d), 4.03 (2H, d), 3.17 (6H, d), 2.41 (2H, q), 2.30 (3H, s), 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-341b157d60874f6baf73271d27514cd3 |
| Source note | uspto-grants-2012_05 |