HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 3616760, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | 1H-indole-6-carboxylic acid | HCID 595230 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 3616760 | HCID 3616760 | 107.3% |
Reaction Steps
In a round-bottomed flask, 5.0 g of indole-6-carboxylic acid, 3.3 g of N,O-dimethylhydroxylamine hydrochloride, 11.9 g of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide and 10 ml of pyridine are placed in 150 ml of tetrahydrofuran. The mixture is stirred at ambient temperature for 40 h. The mixture is concentrated, and the residue is taken up in 150 ml of ethyl acetate and 50 ml of water. The organic phase is washed with 50 ml of a 1N solution of sodium hydroxide and 50 ml of a saturated solution of sodium chloride, dried over magnesium sulphate and then concentrated under reduced pressure. 6.8 g of compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088765B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-d6021ef64e2b49c0bc964dc7747babf1 |
| Source note | uspto-grants-2012_01 |