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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080232Generated: November 3, 2026

Formaldehyde → Quinoline-6-carboxylic acid 4-(benzyl-methyl-amino)-benzylamide

https://huagongshe.com/reaction/2080232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium BicarbonateHCID 516892—
ReactantQuinoline-6-carboxylic acid 4-benzylamino-benzylamideHCID 58388023—
ReactantHCID 58875320HCID 58875320—
CatalystAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
ProductQuinoline-6-carboxylic acid 4-(benzyl-methyl-amino)-benzylamideHCID 5838791735%

Reaction Steps

Quinoline-6-carboxylic acid 4-benzylamino-benzylamide described in Preparation Example E+-3 (30 mg, 82 μmol), formalin (9 μl, 115 μmol), triacetoxy sodium borohydride (25 mg, 115 μmol) and acetic acid (several drops) were suspended in tetrahydrofuran (1 mL), and the solution was stirred at room temperature for 4 hours. An aqueous solution of saturated sodium bicarbonate was added to the reaction suspension at 0° C., which was then extracted with ethyl acetate, the organic layer was washed with brine and dried over anhydrous magnesium sulfate. The solvent was evaporated in vacuo, purification was carried out using thin layer NH silica gel chromatography (hexane:ethyl acetate=1:1), and the title compound (11 mg, 28 μmol, 35%) was obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932272B2
Source datasetuspto-grants-2011_04
ORD IDord-52cde124c1d34d43ac7e34274e28ffd6
Source noteuspto-grants-2011_04