HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510219Generated: October 30, 2026
Sodium ethoxide → HCID 178451642, compound
https://huagongshe.com/reaction/510219
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Methanimidamide, hydrochloride (1:1) | HCID 10313058 | — |
| Reactant | 1-tert-Butyl 4-ethyl 3-oxopiperidine-1,4-dicarboxylate | HCID 15852989 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178451642 | HCID 178451642 | 53.5% |
Reaction Steps
To a solution of 1-tert-butyl 4-ethyl 3-oxopiperidine-1,4-dicarboxylate (2.00 g, 7.39 mmol) in EtOH (37 mL) was added formamidine hydrochloride (910 mg, 11.08 mmol) followed by NaOEt (6.89 mL, 2.68 M in EtOH) dropwise. The mixture was then heated to reflux overnight. The mixture was concentrated in vacuo and then dissolved in a minimum amount of water. The pH was adjusted to pH 7 with 1 N HCl. The aqueous layer was then saturated with solid NaCl and extracted with a combination of EtOAc and DCM. The combined organic extracts were dried over Na2SO4, filtered and concentrated in vacuo. Chromatography on SiO2 eluting with IPA/EtOAc afforded the desired product as a white solid (993 mg, 53%). MS (ESI) mass calcd. C12H12N3O3, 251.13. m/z found 252.1 [M+H]+. 1H NMR (500 MHz, CDCl3): 8.05 (s, 1H), 4.42 (s, 2H), 3.69-3.61 (m, 2H), 2.63 (s, 2H), 1.49 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09096596B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-536af83cdeb646818b592c23ba621b59 |
|---|
| Source note | uspto-grants-2015_08 |
|---|