HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50203Generated: November 1, 2026
4-Methylmorpholine → HCID 18412459, compound
https://huagongshe.com/reaction/50203
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Methyl N-pyridin-2-yl-beta-alaninate | HCID 818199 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | HCID 18412598 | HCID 18412598 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18412459 | HCID 18412459 | — |
Reaction Steps
308 mg (1.0 mmol) of 1-methyl-2-[(4-cyanophenyl)oxymethyl]-5-carboxyimidazo[4,5-b]pyridine were suspended in 5 mL of dimethylformamide and mixed with 303 mg (3.0 mmol) of N-methylmorpholine and 321 mg (1.0 mmol) of O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate. After 10 minutes at room temperature, a solution of 215 mg (1.2 mmol) of methyl N-(2-pyridyl)-3-aminopropionate in 2 mL of dimethylformamide was added, whereupon a clear solution was obtained. After 12 hours at room temperature, the reaction solution was stirred into ice-water. After extracting 3 times with ethyl acetate, the combined organic extracts were washed with a saline solution, dried over sodium sulfate, and evaporated down. The residue obtained was chromatographed on silica gel with dichloromethane/ethanol (90:1 to 25:1). Yield: 165 mg of white powder (35% of theory), C25H12N6O4 (407.50); melting point: 139° C.-140° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06710055B2 |
|---|
| Source dataset | uspto-grants-2004_03 |
|---|
| ORD ID | ord-a03bc704707940258cba8f41bca2b0e9 |
|---|
| Source note | uspto-grants-2004_03 |
|---|