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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410430Generated: October 25, 2026

Triethylamine → 2-chloro-N-methoxy-N-methylpyrimidine-4-carboxamide

https://huagongshe.com/reaction/410430

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantPyBOPHCID 2724699—
Reactant2-Chloropyrimidine-4-carboxylic acidHCID 22135751—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product2-chloro-N-methoxy-N-methylpyrimidine-4-carboxamideHCID 7723135066%

Reaction Steps

To a solution of 2-chloropyrimidine-4-carboxylic acid (3.95 g, 24.9 mmol) and N-methoxymethanamine hydrogen chloride salt (2.43 g, 24.9 mmol) in dichloromethane (15 mL) were added triethylamine (6.95 mL, 50 mmol) and (benzotriazol-1-yloxy)tripyrrolidino-phosphonium hexafluorophosphate (13 g, 24.91 mmol) and stirred for 4 hr. The solution was diluted with EtOAc, washed with brine, dried with MgSO4, filtered, and concentrated to dryness. Purification on silica gel by flash chromatography (0-100% EtOAc/hexanes) afforded 2-chloro-N-methoxy-N-methylpyrimidine-4-carboxamide (3.30 g, 16.37 mmol, 66% yield). MS ESI: [M+H]+ m/z 202.0. 1H NMR (500 MHz, CDCl3) δ 8.75 (d, J=4.6, 1H), 7.48 (d, J=4.6, 1H), 3.77 (s, 3H), 3.35 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759366B2
Source datasetuspto-grants-2014_06
ORD IDord-47084f65e49a46839ea2c8ad76730cb9
Source noteuspto-grants-2014_06