HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfoxide → HCID 9870915, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-[5-(4-Aminonaphthyl)pyridin-2-ylmethyl]morpholine | HCID 10267953 | — |
| Reactant | HCID 12988817 | HCID 12988817 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 9870915 | HCID 9870915 | — |
Reaction Steps
A solution of 5-t-butyl-2-methyl-1-(2,2,2-trichloroethoxycarbonyl)aminobenzene (26 mmol), 1-amino-4-[6-(morpholin-4-ylmethyl)pyridin-3-yl]naphthalene (26 mmol), diisopropylethylamine (3.2 g, 25 mmol) and DMSO (75 mL) is heated to 55-60° C. and held for 1.5 h. To this solution, ethyl acetate (100 mL) is added. The organic layer is washed with brine (4×50 mL), and dried over MgSO4. The solvent is removed under reduced pressure, and residue is crystallized from a suitable solvent such as acetonitrile (50 mL) at 0° C. The product is collected by filtration and recrystallized from a suitable solvent such as isopropanol and dried in vacuum to constant weight.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06894173B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-645ad98b90c8446ba727a219c5ac6736 |
| Source note | uspto-grants-2005_05 |