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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1923968Generated: October 30, 2026

3-Aminoquinoline → HCID 67520955, compound

https://huagongshe.com/reaction/1923968

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-AminoquinolineHCID 11375—
Reactant4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chlorideHCID 2734059—
ReactantHCID 67520362HCID 67520362—
SolventEthyl AcetateHCID 8857—
ProductHCID 67520955HCID 6752095593%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178490B2
Source datasetuspto-grants-2012_05
ORD IDord-de1c8d79b65a4b5cb04fca43a811d3ad
Source noteuspto-grants-2012_05