HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897360Generated: October 30, 2026
Dimethylformamide → HCID 22346305, compound
https://huagongshe.com/reaction/897360
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1-[4-Fluoro-2-(methylsulfanyl)phenyl]methanamine | HCID 16753943 | — |
| Reactant | HCID 22346251 | HCID 22346251 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 22346305 | HCID 22346305 | — |
Reaction Steps
A slurry of dimethyl 8-hydroxy-1,6-naphthyridine-5,7-dicarboxylate (0.25 g, 0.953 mmol), 1-[4-fluoro-2-(methylthio)phenyl]methanamine (0.326 g, 1.91 mmol) and N,N,N-diisopropylethylamine (170 uL, 0.953 mmol) in toluene (4.0 mL) were heated in a pressure tube at 110 degrees C. for 18 hrs. The reaction was incomplete by LCMS analysis and solids remained undissolved. DMF (1 mL) was added to solubilize the reagents and the reaction was again heated in a pressure tube at 110 degrees C. for 18 hrs. Upon cooling to room temperature, the resulting solution was transferred to a round bottom flask and reduced to a small volume. The residue was partitioned between methylene chloride and water. The organic layer was dried with Na2SO4, filtered and reduced in vacuo. The material was crystallized with a small amount of chloroform. The solid was filtered and dried in vacuo to afford the desired compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06921759B2 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-a95db336ab9b49519883259f644cd125 |
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| Source note | uspto-grants-2005_07 |
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