HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82476Generated: October 27, 2026
Nicotinic Acid → 3-Methyl-2-[pyridine-3-carbonyl]-amino-butyric acid methyl ester
https://huagongshe.com/reaction/82476
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nicotinic Acid | HCID 938 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Valine methyl ester | HCID 94285 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-Methyl-2-[pyridine-3-carbonyl]-amino-butyric acid methyl ester | HCID 67325527 | 369.7% |
Reaction Steps
To a solution of L-valine methylester (3.0 g, 2.29 mmol), in DCM (30 mL) were added N-methyl morpholine (11.5 mL, 11.45 mmol), EDCI.HCl (8.7 g, 45.8 mmol) and nicotinic acid (3.3 g, 27.4 mmol). The mixture was allowed to stir at room temperature (25° C.) over 3 h under nitrogen atmosphere. The resulting mixture was diluted with ethyl acetate (200 mL), washed with water (3×100mL) and dried over sodium sulphate. The crude product obtained upon evaporation of the solvent was further purified by silica gel column chromatography to obtain required product as sticky solid (2.0 g, 38%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846721B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-c149b7e51eb84d4c872955058ddfdce3 |
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| Source note | uspto-grants-2014_09 |
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