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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187439Generated: October 30, 2026

Triethylamine → HCID 53792562, compound

https://huagongshe.com/reaction/2187439

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 (110 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 chloroformnethanol 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 numberUS06410530B1
Source datasetuspto-grants-2002_06
ORD IDord-45267ccc4d064edc994f3cb9f82bdf3c
Source noteuspto-grants-2002_06