Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357593Generated: October 31, 2026

Methylamine → N,4-dimethyl-3-(1-morpholinophthalazin-6-yl)benzamide

https://huagongshe.com/reaction/2357593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Methyl-3-(1-morpholinophthalazin-6-yl)benzoic acidHCID 25193063—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventThionyl ChlorideHCID 24386—
ProductN,4-dimethyl-3-(1-morpholinophthalazin-6-yl)benzamideHCID 68452282—

Reaction Conditions

Temperature65 °C

Reaction Steps

4-Methyl-3-(1-morpholinophthalazin-6-yl)benzoic acid (100 mg, 286 μmol) was dissolved in thionyl chloride (5.7 mL) and heated to 65° C. for 1 h. The reaction was then concentrated in vacuo, dissolved in tetrahydrofuran 99.9% (5.7 mL) and diisopropylethylamine (150 μL, 859 μmol) and methylamine, 2.0 m solution in THF (0.7 mL) were added. The reaction mixture was stirred for 3 h at ambient temperature. The reaction mixture was diluted with 50 mL of EtOAc, added to an addition funnel and partitioned with sodium bicarbonate (saturated, aqueous). The organic layers were washed 3 times with 50 mL of sodium bicarbonate (saturated, aqueous), dried over sodium sulfate, and concentrated via rotovap to give a crude product. After purification by chromatography, the title compound was obtained. Found MS (ES+): 363(M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759337B2
Source datasetuspto-grants-2010_07
ORD IDord-8953f0acc63446c1a84774c219f57d31
Source noteuspto-grants-2010_07