Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloranil | HCID 8371 | — |
| Reactant | 2-Methoxybenzaldehyde | HCID 8658 | — |
| Reactant | HCID 59645484 | HCID 59645484 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178472256 | HCID 178472256 | 71% |
Reaction Steps
A solution of diethyl [3,4-diamino-2-(methoxycarbonyl)phenyl]malonate (4.39 g, 13.5 mmol), 2-methoxybenzaldehyde (1.97 g, 14.5 mmol) and p-chloranil (6.10 g, 14.5 mmol) in MeCN (135 mL) was stirred at room temperature for 22 h. The resulting suspension was filtered and the solid recovered was washed with MeCN (filtrate 1 kept). The solid was dissolved in EtOAc (800 mL) and the resulting solution was successively washed with aqueous 1N NaOH solution (3×150 mL), water (150 mL) and brine (100 mL), dried (MgSO4), filtered and concentrated under reduced pressure. The resulting solid was triturated with hexane:EtOAc (1:1; 135 mL) to give the title compound (4.22 g) as a white solid (filtrate 2 kept). The filtrates 1 and 2 were combined and concentrated under reduced pressure. The residue was treated as the initial solid but the residue after washings was concentrated and purified by flash chromatography (10-40μ silica gel; hexane:EtOAc 1:1) before being triturated with hexane:EtOAc (3:2; 35 mL) to give an additional 0.72 g amount (total of 4.96 g, 83% yield) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07323567B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-8bc6520a868846ea9501334b697e2239 |
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| Source note | uspto-grants-2008_01 |
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