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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2044840Generated: October 26, 2026

4-Methoxybenzylamine → N-(4-methoxybenzyl)(8-methyl-2-(2-(trifluoromethyl)phenyl)quinolin-3-yl)methanamine

https://huagongshe.com/reaction/2044840

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzylamineHCID 75452—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant8-Methyl-2-(2-(trifluoromethyl)phenyl)quinoline-3-carbaldehydeHCID 57556160—
Solvent1,2-DichloroethaneHCID 11—
ProductN-(4-methoxybenzyl)(8-methyl-2-(2-(trifluoromethyl)phenyl)quinolin-3-yl)methanamineHCID 57707763—

Reaction Steps

Prepared according to Procedure F using 8-methyl-2-(2-(trifluoromethyl)phenyl)-quinoline-3-carbaldehyde (1 g, 3.17 mmol), DCE (16 mL), PMBNH2 (0.62 mL, 4.75 mmol, 1.5 eq), and NaBH(OAc)3 (2.0166 g, 9.52 mmol, 3 eq). After purification, N-(4-methoxybenzyl)(8-methyl-2-(2-(trifluoromethyl)phenyl)-quinolin-3-yl)methanamine was obtained as light yellow syrup. 1H NMR (DMSO-d6) δ ppm 8.48 (1 H, s), 7.87 (2 H, t, J=7.2 Hz), 7.64-7.77 (2 H, m), 7.48-7.62 (3 H, m), 7.14 (2 H, d, J=8.6 Hz), 6.81 (2 H, d, J=8.6 Hz), 3.71 (3 H, s), 3.44-3.62 (4 H, m), 2.61 (3 H, s), 2.54 (1 H, s). Mass Spectrum (ESI) m/e=437.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586739B2
Source datasetuspto-grants-2013_11
ORD IDord-bdb1ea55a4e84bcab495fda0f6108eed
Source noteuspto-grants-2013_11