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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537473Generated: October 31, 2026

6-Chloronicotinic acid → 6-Chloro-N-methoxy-N-methylnicotinamide

https://huagongshe.com/reaction/537473

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Chloronicotinic acidHCID 79222—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantMethoxymethanamine hydrochlorideHCID 21959107—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
Product6-Chloro-N-methoxy-N-methylnicotinamideHCID 1143559790.3%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 6-chloronicotinic acid (2.0 g, 12.7 mmol) in DMF (20 mL) was added TBTU (6.11 g, 19.0 mmol), di-iso-propylethylamine (4.9 g, 38.1 mmol), and N-methoxymethylamine hydrochloride (1.48 g, 15.2 mmol). The reaction mixture was stirred at 25° C. overnight. The reaction solution was poured into brine (40 mL) and extracted with ethyl acetate (40 mL*2). The organic layer was dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by silica gel chromatography to give 6-chloro-N-methoxy-N-methylnicotinamide (2.3 g) as an oil. 1H NMR (400 MHz, CDCl3) δ 8.70 (d, J=2.0 Hz, 1H), 7.95 (dd, J=2.4, 8.4 Hz, 1H), 7.32 (d, J=8.0 Hz, 1H), 3.49 (s, 3H), 3.32 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859591B2
Source datasetuspto-grants-2014_10
ORD IDord-b2a95619d93c46219b57a39b9341d37a
Source noteuspto-grants-2014_10