HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 2-aminopyridine-3-carboxylate → HCID 178515099, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 2-aminopyridine-3-carboxylate | HCID 351633 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 58923367 | HCID 58923367 | — |
| Solvent | 1-Hexanol | HCID 8103 | — |
| Product | HCID 178515099 | HCID 178515099 | 2.1% |
Reaction Steps
5-Morpholin-4-yl-benzene-1,3-diol (345 mg 1.77 mmol), TsOH.H2O (30 mg, 0.20 mmol), and 2-aminonicotinic acid methyl ester (269 mg, 1.77 mmol) were heated at 160° C. in hexanol (5 mL) for 12 hours. Upon cooling, the mixture was purified via flash chromatography CH2Cl2/MeOH (95:5), followed by a second flash column eluting with Et2OAc/hexanes (7:3) to provide 11 mg (2%) of the product. 1H NMR (CDCl3, 400 MHz) δ: 13.5 (s, 1H), 8.80 (br s, 1H), 8.62 (d, 1H), 7.25 (dd, 1H), 6.22 (d, 1H), 6.04 (s, 1H), 5:97 (s, 1H), 3.86-3.83 (m, 4H), 3.40-3.35 (m, 4H). LRMS (APCI, positive): Da/e 296.4 (m−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08404681B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-45ad2f8dac534f37b59170332cc0e9fb |
| Source note | uspto-grants-2013_03 |