HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 69057960, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 5-Hydroxyindole-2-carboxylic acid | HCID 88958 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-Aminopyridine-2-carbonitrile | HCID 3871395 | — |
| Reactant | 1H-Imidazolium, 2-chloro-4,5-dihydro-1,3-dimethyl-, chloride | HCID 10986715 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 69057960 | HCID 69057960 | — |
Reaction Steps
At 0° C., 2-chloro-1,3-dimethyl-imidazolinium chloride (1.0 g) was added to a chloroform (6.0 mL)/pyridine (6.0 mL) mixed solution of 5-amino-2-cyanopyridine (500 mg) and 5-hydroxyindole-2-carboxylic acid (1.1 g), and stirred for 3 hours, and further stirred overnight at room temperature. Aqueous sodium hydrogencarbonate solution was added to the reaction liquid to stop the reaction, and this was extracted with chloroform. The organic layer was washed with water and saturated saline water, and then dried with anhydrous sodium sulfate. The organic layer was concentrated under reduced pressure, and the resulting crystal was washed with chloroform to obtain the entitled compound (1.4 g) as a pale red solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07531668B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-dd1afc25339d4bd0a78c093b7d8b3fc2 |
| Source note | uspto-grants-2009_05 |