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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187412Generated: October 31, 2026

Pyridine → Diethylether hexane

https://huagongshe.com/reaction/2187412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant(R)-2-amino-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydronaphthaleneHCID 53960413—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductDiethylether hexaneHCID 21584099104.4%
Product(R)-N-[8-(4-Methylpiperazin-1-yl)-1,2,3,4-tetrahydro-2-naphthyl]trifluoroacetamideHCID 54128870—

Reaction Steps

To an ice-cooled solution of (R)-2-amino-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydronaphthalene (120 mg, 0.49 mmol), pyridine (100 μL, 1.2 mmol) and 4-dimethylaminopyridine (20 mg, 0.16 mmol) in methylene chloride (10 mL) was added dropwise trifluoroacetic anhydride (72 μL, 0.51 mmol). After the addition the reaction was allowed to stir at ambient temperature for 1 h and was then washed with water. The methylene chloride phase was dried (Na2SO4), filtered and evaporated in vacuo. The residue was purified on a silica gel column using ethyl acetate/methanol/concentrated ammonium hydroxide (96:4:0.5) as the eluent. This gave after crystallization from diethyl ether/hexane 41 mg (24% yield) of the title compound as white crystals: mp 158-159° C.; [α]21D +39° (c 0.25, chloroform); EIMS (70 eV) m/z (relative intensity) 341 (82, M30).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410530B1
Source datasetuspto-grants-2002_06
ORD IDord-5ce8f91333d94c96b07352dc6e6479a5
Source noteuspto-grants-2002_06