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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1954806Generated: November 4, 2026

Triethylamine → HCID 53792562, compound

https://huagongshe.com/reaction/1954806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Benzylbenzoic acidHCID 136429—
Reactant(R)-2-amino-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydronaphthaleneHCID 53960413—
SolventDichloromethaneHCID 6344—
SolventThionyl ChlorideHCID 24386—
ProductHCID 53792562HCID 53792562—

Reaction Steps

4-Benzylbenzoic acid (0.50 g, 2.4 mmol) was dissolved in thionyl chloride (10 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 (100 mg, 0.46 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 (10 mg, 0.44 mmol) and triethylamine (90 μL, 0.65 mmol) in methylene chloride (25 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: 130 mg (62%) of the title compound as white crystals: mp 191-192° C.; [α]21D -39° (c 1.0, chloroform); EIMS (70 eV) m/z (relative intensity) 439 (28, M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124283
Source datasetuspto-grants-2000_09
ORD IDord-7ec5bf153e33475a82e3922cc7ef7563
Source noteuspto-grants-2000_09