HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-[(3-Methoxypropyl)amino]-6-(1-methylethyl)pyridine-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 4-[(3-methoxypropyl)amino]-6-(1-methylethyl)pyridine-3-carboxylate | HCID 59625354 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-[(3-Methoxypropyl)amino]-6-(1-methylethyl)pyridine-3-carboxylic acid | HCID 59625668 | 126.8% |
Reaction Steps
To a solution of ethyl 4-[(3-methoxypropyl)amino]-6-(1-methylethyl)pyridine-3-carboxylate (263 mg) in ethanol (5 ml) was added 2 M aqueous sodium hydroxide solution (0.94 ml) and the mixture was stirred at room temperature for 15 hr. The reaction mixture was adjusted to pH 7 with 1 M hydrochloric acid, and the solvent was evaporated under reduced pressure. The residue was suspended in ethanol, and the precipitated inorganic salt was filtered off. The filtrate was concentrated under reduced pressure to give the object compound (300 mg) as a mixture of inorganic salts.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08329691B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-83ff2e2cb3d041feb2d1447d656acba3 |
| Source note | uspto-grants-2012_12 |