HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524049Generated: October 29, 2026
Diisopropylethylamine → Ethyl 6-chloro-4-(methylamino)pyridine-3-carboxylate
https://huagongshe.com/reaction/524049
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ethyl 4,6-dichloropyridine-3-carboxylate | HCID 600045 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 6-chloro-4-(methylamino)pyridine-3-carboxylate | HCID 20627001 | 96.5% |
Reaction Steps
To a solution of ethyl 4,6-dichloronicotinate (5.0 g, 22.7 mmol) in acetonitrile (50 mL) was added methylamine hydrochloride salt (1.84 g, 27.2 mmol) and diisopropylethylamine (14.6 g, 113.6 mmol), and the reaction mixture was heated at 70° C. overnight. LCMS showed the reaction was completed. The reaction was cooled to RT, quenched with water (50 mL) and extracted with ethyl acetate (3×100 mL). The organic layers were separated, combined, washed with water (50 mL) and brine (100 mL), dried over sodium sulfate, filtered, and concentrated to afford the title compound (4.7 g, crude), which was directly used in the next step without further purification. MS (ES+) C9H11ClN2O2 requires: 214, 216. found: 215, 217 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09340514B2 |
|---|
| Source dataset | uspto-grants-2016_05 |
|---|
| ORD ID | ord-d8702735c4f0487aa7345eba28133770 |
|---|
| Source note | uspto-grants-2016_05 |
|---|