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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333065Generated: October 30, 2026

Triethylamine → (E)-4,4,5,5,5-Pentafluoro-N-[3-[(2-methyl-4-quinolyl)amino]propyl]pent-2-enamide

https://huagongshe.com/reaction/333065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
ReactantAluminaHCID 9989226—
ReactantN1-(2-Methylquinolin-4-YL)propane-1,3-diamine hydrochlorideHCID 17999421—
Reactant(2E)-4,4,5,5,5-Pentafluoro-2-pentenoic acidHCID 86691160—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
Product(E)-4,4,5,5,5-Pentafluoro-N-[3-[(2-methyl-4-quinolyl)amino]propyl]pent-2-enamideHCID 86691162—

Reaction Steps

(E)-4,4,5,5,5-Pentafluoropent-2-enoic acid (38 mg, 0.2 mmol) and HBTU (76 mg, 0.2 mmol) were dissolved in a 1:1 mixture of anhydrous DMF and anhydrous acetonitrile (2 ml), after 5 minutes triethylamine (82 μl, 0.6 mmol) and N-(2-methyl-4-quinolyl)propane-1,3-diamine hydrochloride (48 mg, 0.24 mmol) was added and stirring was continued for 3 hours. To the mixture basic aluminium oxide was added, stirring was continued for one hour, the mixture was filtered and the filtrate was evaporated to dryness under reduced pressure. The residue was purified by preparative HPLC (gradient of water containing 0.1% NH3 and acetonitrile) to yield 28.4 mg (0.076 mmol, 38%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877934B2
Source datasetuspto-grants-2014_11
ORD IDord-0d5bac1625eb4331b0eff6a63b8e83d3
Source noteuspto-grants-2014_11