HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → HCID 15616388, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Quinuclidine, 3-amino-, dihydrochloride | HCID 197853 | — |
| Reactant | HCID 287116 | HCID 287116 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 15616388 | HCID 15616388 | — |
Reaction Steps
The above compound was prepared, following the procedure of Example 14b, from 3-aminoquinuclidine dihydrochloride(1.0 g, 5 mmol), 2-pyridoylurea (0.82 g, 5 mmol) and di-isopropylethylamine (1.3 g, 10 mmol) in pyridine (20 ml) by refluxing for 4 days. The pyridine was evaporated and the residue partitioned between ether and 10% aqueous w/v citric acid. The mixture was filtered, the aqueous phase washed with ether, then basified with potassium carbonate to precipitate the title compound (0.60 g) which was converted to the 1:1 fumarate, mp 202°-203° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04983600 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-6c5c57195731430ba9ae7a234fe3d815 |
| Source note | uspto-grants-1991_01 |