HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791357Generated: October 27, 2026
Triethylamine → Methyl 1-(pyridin-2-ylmethyl)piperidine-2-carboxylate
https://huagongshe.com/reaction/1791357
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Pyridinecarboxaldehyde | HCID 14273 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Methyl Pipecolinate Hydrochloride | HCID 13246231 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | Methyl 1-(pyridin-2-ylmethyl)piperidine-2-carboxylate | HCID 11776206 | 93.6% |
Reaction Steps
Methyl pipecolinate hydrochloride (9.0 g, 50 mmol) was mixed with pyridine-2-carbaldehyde (5.4 g, 50 mmol) and triethylamine (5.05 g, 50 mmol) in dichloroethane (180 mL) at room temperature. Sodium triacetoxyborohydride (14.8 g, 70 mmol) was added in one portion. After the reaction mixture was stirred at room temperature for 1.5 h, saturated sodium carbonate was added. Then the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried with sodium sulfate, filtered and concentrated to give 10.9 g (93.6%) of the title compound as a pale brown oil. 1H NMR (CDCl3), δ(ppm): 8.53 (d, 1H), 7.65 (td, 1H), 7.49 (d, 1H), 7.14 (t, 1H), 3.89 (d, 1H), 3.73 (s, 3H), 3.68 (d, 1H), 3.25 (dd, 1H), 2.97 (m, 1H), 2.25 (m, 1H), 1.85 (m, 2H), 1.30-1.76(m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07074809B2 |
|---|
| Source dataset | uspto-grants-2006_07 |
|---|
| ORD ID | ord-c969145559604c7d8937ea3bf6a22d15 |
|---|
| Source note | uspto-grants-2006_07 |
|---|