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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187441Generated: October 30, 2026

Triethylamine → HCID 9824760, compound

https://huagongshe.com/reaction/2187441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-(Trifluoroacetyl)benzoic acidHCID 143579—
Reactant(R)-2-amino-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydronaphthaleneHCID 53960413—
SolventDichloromethaneHCID 6344—
SolventThionyl ChlorideHCID 24386—
ProductHCID 9824760HCID 9824760—

Reaction Steps

4-(Trifluoroacetyl)benzoic acid (0.50 g, 2.4 mmol) was dissolved in thionyl chloride (15 mL) and heated at reflux for 20 min. The excess of thionyl chloride was evaporated in vacuo, the residue was treated with toluene and again the solvent was removed in vacuo. Crude acid chloride (97 mg, 0.43 mmol) was dissolved in methylene chloride (5 mL) and added dropwise to an ice-cooled solution of (R)-2-amino-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydronaphthalene (100 mg, 0.41 mmol) and triethylamine (85 μL, 0.61 mmol) in methylene chloride (35 mL). After the addition, the reaction was allowed to stir at ambient temperature for 15 min and was then washed with dilute aqueous sodium hydrogen carbonate. The phases were separated and the organic phase was dried (Na2SO4), filtered and evaporated in vacuo to give a crude product which was purified on a silica gel column using chloroform/ethanol saturated with NH3 (100:3) as the eluent. Yield: 98 mg (54%) of the title compound as slightly yellow crystals: mp 91-93° C.; [α]21D −47° (c 1.0, chloroform); EIMS (70 eV) m/z (relative intensity) 453 (27, M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410530B1
Source datasetuspto-grants-2002_06
ORD IDord-e03321460ab94be78d4e8b4cdaec8122
Source noteuspto-grants-2002_06