HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744962Generated: October 30, 2026
Ethyl 4-oxo-1-piperidinecarboxylate → HCID 68704856, compound
https://huagongshe.com/reaction/1744962
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 4-oxo-1-piperidinecarboxylate | HCID 34767 | — |
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 68704856 | HCID 68704856 | — |
Reaction Steps
To a round bottomed flask was loaded 8.56 grams of 4-oxo-piperidine-1-carboxylic acid ethyl ester, 10.3 ml of dimethylformamide dimethylacetal, and the mixture was refluxed at 90° C. for two hours. Then it was poured into 75 ml water and extracted with 2×250 ml dichloromethane. The combined organic layers was washed with 50 ml brine and dried over magnesium sulfate. Filter off the drying agent and concentrate gave 28 grams of 3-Dimethylaminomethylene-4-oxo-piperidine-1-carboxylic acid ethyl ester. This material (12.8 grams) was then loaded into a round bottomed flask along with 3.42 grams of (5-Amino-1H-[1,2,4]triazol-3-yl)-methanol and 100 ml 2-methoxyethanol. The mixture was refluxed for 18 hours. Then it was cooled down to 23° C. and concentrated to 5 ml. Then 50 ml ethyl ether was added and the precipitate was filtered and vaccum dried to yielded 1.5 grams of product. MS: 278.1 (M+H). H-NMR(CDCL3): δ 8.60(s, 1H), 4.98(s, 2H), 4.78(s, 2H, CH2), 4.22(q, 2H, J=4.8 Hz), 3.75 (t, 2H, CH2, J=4 Hz), 3.51 (t, 2H, J=4 Hz), 1.32 (m, 3H, CH3, J=4.8 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07018997B2 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-1a420ef8cd054f569b30ae8c2a5bd96f |
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| Source note | uspto-grants-2006_03 |
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