HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 15030209, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | O-methylhydroxylammonium chloride | HCID 11639 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 2-[6-[(Quinolin-2-yl)methoxy]naphthalen-2-yl]propanoic acid | HCID 11725870 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15030209 | HCID 15030209 | — |
Reaction Steps
To a mixture of the acid of Example 1 (2.32 g, 6.5 mmol), 0-methylhydroxylamine hydrochloride (0.54 g, 6.5 mmol) and 1-ethyl-3-[3-(dimethylamino)propyl]carbodiimide (1.25 g, 6.5 mmol) in tetrahydrofuran (100 ml) is added triethylamine (2.0 ml, 2 equiv). After overnight stirring at room temperature, the solvent is removed and methylene chloride is added. This is followed by sequential washings with 0.05N hydrochloric acid and water (2x). After drying over magnesium sulfate, the solvent is removed to afford a crude solid which is recrystallized from ethyl acetate to afford a white crystalline solid, 0.6 g(24%), m.p. 162°-164° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05250693 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-81c1c36ed3964f3b965bfa807758f148 |
| Source note | uspto-grants-1993_10 |