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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Methyl-3-(1-morpholinophthalazin-6-yl)benzoic acid | HCID 25193063 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | N,4-dimethyl-3-(1-morpholinophthalazin-6-yl)benzamide | HCID 68452282 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07759337B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-8953f0acc63446c1a84774c219f57d31 |
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| Source note | uspto-grants-2010_07 |
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