HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 3-(6-Methyl-pyridin-2-yl)-3-(2-oxo-pyrrolidin-1-ylimino)-propionic Acid Ethyl Ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 1-Aminopyrrolidin-2-one hydrochloride | HCID 21992845 | — |
| Reactant | Ethyl 3-(6-methylpyridin-2-yl)-3-oxopropanoate | HCID 59710028 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(6-Methyl-pyridin-2-yl)-3-(2-oxo-pyrrolidin-1-ylimino)-propionic Acid Ethyl Ester | HCID 59710033 | — |
Reaction Steps
Add 1-aminopyrrolidin-2-one hydrochloride (Zubek, A. Z. Chem. 1969, 9(2), 58; 99.4 g, 0.73 mol) to a 3 L flask equipped with mechanical stirrer and nitrogen inlet. Add 3-[6-methyl-(pyridin-2-yl)]-3-oxo-propionic acid ethyl ester (Preparation 1, Part A; 154 g, 0.66 mol), and pyridine (280 mL). Stir the reaction mixture at room temperature for 20 h. Dilute the mixture with water (200 mL) and extract with toluene (2×250 mL). Combine the organic layers, filter, and concentrate in vacuo to yield the subtitled product (201 g) as a dark oil. MS (ES) m/z=290 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07511056B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-0f2ff0e0340d4868a4cf4ff638611eac |
| Source note | uspto-grants-2009_03 |