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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070645Generated: October 31, 2026

4-Chlorobenzylamine → HCID 10159541, compound

https://huagongshe.com/reaction/1070645

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorobenzylamineHCID 66036—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 22397176HCID 22397176—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 10159541HCID 1015954167%

Reaction Steps

At 0° C., a solution of 2.0M AlCl3 in toluene (0.14 mL) is added to a solution of 4-chlorobenzylamine (0.044 mL) in CH2Cl2 (5 mL). The compound from ethyl-1-methyl-6-(4-morpholinylmethyl)-4-oxo-1,4-dihydro[1,7]naphthyridine-3-carboxylate (Preparation 46, 0.058 g) is added and the mixture allowed to stir at room temperature for 3 hours at which time the mixture is partitioned between CH2Cl2 (30 mL) and water (30 mL). The organics are dried with Na2SO4, filtered and the solvent evaporated. The remaining solid is chromatographed with MeOH/CH2Cl2 (1-4%) to obtain 0.049 g (67%) of the title compound as an off-white solid. Physical characteristics: MS (ESI+) m/z 427 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903097B2
Source datasetuspto-grants-2005_06
ORD IDord-699ee55737634316b8aa80fec281cb06
Source noteuspto-grants-2005_06