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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1349485Generated: November 1, 2026

Methylamine → 3-Benzyloxy-1-(2,2-dimethoxyethyl)-5-methylcarbamoylmethyl-4-oxo-1,4-dihydropyridine-2-carboxylic acid 3-chlorobenzylamide

https://huagongshe.com/reaction/1349485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant[5-Benzyloxy-6-(3-chlorobenzylcarbamoyl)-1-(2,2-dimethoxyethyl)-4-oxo-1,4-dihydropyridin-3-yl]acetic acidHCID 21091365—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
Product3-Benzyloxy-1-(2,2-dimethoxyethyl)-5-methylcarbamoylmethyl-4-oxo-1,4-dihydropyridine-2-carboxylic acid 3-chlorobenzylamideHCID 5885915285.8%

Reaction Steps

To a solution of [5-benzyloxy-6-(3-chlorobenzylcarbamoyl)-1-(2,2-dimethoxyethyl)-4-oxo-1,4-dihydropyridin-3-yl]acetic acid (25 mg) obtained in Example 191, Step 1 in dimethylformamide (0.2 ml), were successively added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (19 mg), 1-hydroxybenzotriazole hydrate (15 mg) and methylamine (2M tetrahydrofuran solution) (0.073 ml), and the mixture was stirred at room temperature for 2 hr. The obtained reaction mixture was applied as it was to silica gel thin layer chromatography (chloroform:methanol=10:1) and crystallized from ethyl acetate-diisopropyl ether to give 3-benzyloxy-1-(2,2-dimethoxyethyl)-5-methylcarbamoylmethyl-4-oxo-1,4-dihydropyridine-2-carboxylic acid 3-chlorobenzylamide (22 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07211572B2
Source datasetuspto-grants-2007_05
ORD IDord-cd8a5de3a2344d9caf27b9a8547dc6fb
Source noteuspto-grants-2007_05