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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2063974Generated: October 27, 2026

6-Bromomethyl-2-chloronicotinic acid methyl ester → 2-Chloro-6-diformylaminomethylnicotinic acid methyl ester

https://huagongshe.com/reaction/2063974

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromomethyl-2-chloronicotinic acid methyl esterHCID 21083280—
ReactantCID 86637722HCID 86637722—
SolventDimethylformamideHCID 6228—
Product2-Chloro-6-diformylaminomethylnicotinic acid methyl esterHCID 5832453244%

Reaction Steps

To a solution of crude 6-bromomethyl-2-chloronicotinic acid methyl ester (235 g) in DMF (500 mL) was added sodium diformamide (82 g, 0.878 mol) portion wise, maintaining the temperature below 30° C., and the reaction mixture stirred at room temperature for 16 hours (N.B. the reaction mixture rapidly darkened and a small exotherm was observed). The reaction mixture was concentrated in vacuo and the residue dissolved in ethyl acetate (400 mL). The resultant solution was washed with water (2×400 mL) and the aqueous layer extracted with ethyl acetate (2×300 mL). The combined organic extracts were washed with brine (200 mL), dried (MgSO4) and concentrated in vacuo. The resultant residue was dry-loaded onto silica (200 g) and the residue subjected to flash chromatography (SiO2 300 g, 10-30% ethyl acetate in cyclohexane) to yield the title compound as a yellow solid (90.2 g, 44% over two steps). 1H NMR (CDCl3, 400 MHz) 8.46 (2H, br s), 7.56 (1H, d, J=7.7 Hz), 6.66 (1H, d, J=7.9 Hz), 4.39 (2H, br s), 3.36 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288408B2
Source datasetuspto-grants-2012_10
ORD IDord-2336cd6d62e441e08f80ae2b95c39ef9
Source noteuspto-grants-2012_10