HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Aminoquinoline → HCID 67520955, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Aminoquinoline | HCID 11375 | — |
| Reactant | 4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride | HCID 2734059 | — |
| Reactant | HCID 67520362 | HCID 67520362 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67520955 | HCID 67520955 | 93% |
Reaction Steps
To a solution of (2R)-2-{[(tert-butoxy)carbonyl]amino}-4-[4-(trifluoromethyl)phenyl]butanoic acid V (0.97 g, 2.79 mmol) and 3-aminoquinoline VI (0.45 g, 3.10 mmol) in ethyl acetate (30 mL) was added DMT-MM (1.0 g, 3.63 mmol). After being stirred at r.t. overnight, the reaction was washed with water, 1N HCl, aq. sat. NaHCO3, water and dried over Na2SO4. The solvent was removed under reduced pressure to afford tert-butyl N-[(1R)-1-[(quinolin-3-yl)carbamoyl]-3-[4-(trifluoromethyl)phenyl]propyl]carbamate (1.23 g, 2.59 mmol, 93% yield). ESIMS found for C25H26F3N3O3 m/z 474 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08178490B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-de1c8d79b65a4b5cb04fca43a811d3ad |
| Source note | uspto-grants-2012_05 |