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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392073Generated: October 29, 2026

Triethylamine → HCID 22662758, compound

https://huagongshe.com/reaction/392073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 22662739HCID 22662739—
Reactant4-Piperidinylmethyl 4-amino-5-chloro-2-methoxybenzoateHCID 22662757—
SolventDimethylformamideHCID 6228—
ProductHCID 22662758HCID 2266275826%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 1-chloro-(4-fluorophenoxy)propane (2.3 g), intermediate 11 (3 g) and N,N-diethylethanamine (2.8 ml) in DMF (50 ml) was stirred for 48 hours at 70° C. The reaction mixture was cooled and the solvent was evaporated. The residue was partitioned between DCM and water. The organic layer was separated, washed with water, dried, filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH 95/5). The pure fractions were collected and the solvent was evaporated. The residue was crystallized from ACN (0° C.). The precipitate was filtered off and dried (vacuum; 50° C.), yielding 1.17 g (26%) [1-[3-(4-fluorophenoxy)propyl]-4-piperidinyl]methyl 4-amino-5-chloro-2-methoxybenzoate (compound 1, mp. 140.0° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06800628B2
Source datasetuspto-grants-2004_10
ORD IDord-a1f4f59beea84b7a9e6172d00909172b
Source noteuspto-grants-2004_10