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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279266Generated: November 3, 2026

Diisopropylethylamine → HCID 23377662, compound

https://huagongshe.com/reaction/1279266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-CHLORO-6-METHYL-3-NITROPYRIDIN-2(1H)-ONEHCID 11435412—
ReactantHCID 18629275HCID 18629275—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 23377662HCID 23377662—

Reaction Conditions

Temperature25 °C

Reaction Steps

1-methoxymethyl-3-methoxypropylamine (4.19 g, 22.3 mmol), and 4-chloro-6-methyl-3-nitropyridone (3.87 g, 22.3 mmol) were mixed in CH3CN (70 mL) and diisopropyl-ethylamine (9.4 mL, 53.6 mmol) was added. The reaction was stirred at 25° C. for 16 h and at reflux for 2.5 h. The solvent was stripped off and the residue was dissolved in CH2Cl2 (150 mL) and the CH2Cl2 was washed with water (80 mL). The water was extracted with CH2Cl2 (50 mL) and the combined organic extracts were dried (MgSO4) and stripped in vacuo. The residue was crystallized from EtOAc and washed with 40% EtOAc/hexanes to give the product, (4.8 g, 75%). NMR(DMSO)d 9.13 (d, 1H, J=8.8 Hz), 5.9 (s, 1H), 3.92-4.02 (m, 1H), 3.20-3.25 (m, 2H), 3.28-3.4 (m, 2H), 3.25 (s, 3H), 3.18 (s, 3H), 2.09 (s, 3H), 1.65-1.90 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448261B1
Source datasetuspto-grants-2002_09
ORD IDord-a9f71c85674a43459e11881bdacfdb52
Source noteuspto-grants-2002_09