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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888381Generated: October 30, 2026

1,2-Dichloroethane → Methyl 3-[(methylamino)carbonyl]-5-(5-methylpyridin-2-yl)benzoate

https://huagongshe.com/reaction/888381

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantAmmoniaHCID 222—
Reactant1,4-DioxaneHCID 31275—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-(Methoxycarbonyl)-5-(5-methylpyridin-2-yl)benzoic acidHCID 68499417—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-[(methylamino)carbonyl]-5-(5-methylpyridin-2-yl)benzoateHCID 6849678893.9%

Reaction Steps

To a solution of 3-(methoxycarbonyl)-5-(5-methylpyridin-2-yl)benzoic acid (1.85 g, 6.82 mmol) in N,N-dimethylformamide (20 mL) was added 2 M ammonia in dioxane (10.2 mL, 20.4 mmol), EDC (2.61 g, 13.6 mmol), HOBT (2.09 g, 13.6 mmol) and N,N-diisopropylethylamine (4.76 mL, 27.3 mmol). After 16 h, the reaction was concentrated and the residue was dissolved in 200 ml of dichloromethane. The mixture was washed with 100 mL of saturated aqueous sodium bicarbonate solution (2×) and brine (100 ml). The combined organic extracts were dried over sodium sulfate, filtered and concentrated. The residue was purified by silica gel chromatography (1% ethyl acetate/hexane→60% ethyl acetate/hexane) to give the title compound (1.82 g). MS 285.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247401B2
Source datasetuspto-grants-2012_08
ORD IDord-56d7b4349c594464979d9dc1d0a41253
Source noteuspto-grants-2012_08