HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82720Generated: October 25, 2026
Diisopropylethylamine → 4-amino-N-(6-chloropyridin-2-yl)-1,2,5-oxadiazole-3-carboxamide
https://huagongshe.com/reaction/82720
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Amino-6-chloropyridine | HCID 206246 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Amino-1,2,5-oxadiazole-3-carboxylic acid | HCID 547454 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-amino-N-(6-chloropyridin-2-yl)-1,2,5-oxadiazole-3-carboxamide | HCID 58558321 | — |
Reaction Steps
A solution of 4-amino-1,2,5-oxadiazole-3-carboxylic acid (0.4 g, 3.1 mmol) and 6-chloropyridin-2-amine (0.56 g, 4.3 mmol) in N,N-dimethylformamide (6.2 mL) was treated with N,N,N′,N′-tetramethyl-O-(7-azabenzotriazol-1-yl)uronium hexafluorophosphate (1.4 g, 3.7 mmol) followed by N,N-diisopropylethylamine (0.76 mL, 4.3 mmol) at 0° C. The reaction mixture was stirred at 25° C. for 2 h, poured into saturated NaHCO3 (50 mL) and extracted with ethyl acetate (100 mL). The organic layer was separated and washed with brine (25 mL), dried with sodium sulfate, filtered, and concentrated to a crude solid. The crude solid was washed with ethyl acetate and filtered. The filtrate was concentrated and purified on silica gel to give the desired product with some impurities. The impurities were removed by washing the solid with chloroform to yield the desired product (65 mg, 9%). LCMS for C8H7ClN5O2 (M+H)+: m/z=240.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08846726B2 |
|---|
| Source dataset | uspto-grants-2014_09 |
|---|
| ORD ID | ord-f6d3c17003254f4097d6eb0e3f792084 |
|---|
| Source note | uspto-grants-2014_09 |
|---|