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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187448Generated: October 30, 2026

Triethylamine → HCID 54131278, compound

https://huagongshe.com/reaction/2187448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4'-ethyl-4-biphenylcarboxylic acidHCID 521801—
Reactant(R)-2-amino-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydronaphthaleneHCID 53960413—
SolventDichloromethaneHCID 6344—
SolventThionyl ChlorideHCID 24386—
ProductHCID 54131278HCID 54131278—

Reaction Steps

4′-Ethyl-4-biphenylcarboxylic acid (1.0 g, 4.4 mmol) was dissolved in thionyl chloride (15 mL) and heated at reflux for 1 h. 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 (130 mg, 0.53 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 (120 mg, 0.48 mmol) and triethylamine (99 μL, 0.72 mmol) in methylene chloride (20 mL) . After the addition, the reaction was allowed to stir at ambient temperature for 15 min and was then washed with water. 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 (100:4) as the eluent. Yield: 140 mg (53%) of the title compound as white crystals: mp 234-235° C.; [α]21D −73° (c 1.0, chloroform); EIMS (70 eV) m/z (relative intensity) 453 (10, M+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410530B1
Source datasetuspto-grants-2002_06
ORD IDord-cb88c65063e34e4fb261c38999b180aa
Source noteuspto-grants-2002_06