Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 13604735 | HCID 13604735 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | HCID 86628739 | HCID 86628739 | — |
| Product | HCID 13604742 | HCID 13604742 | — |
Reaction Steps
4.2 g (15 millimoles) of 6-[p-(3-formylpyrrol-1-yl)-phenyl]4, 5-dihydro-5-methylpyridazin-3-one (compound from Example 1A) in 30 ml of methanol were stirred with 3.36 g (30 millimoles) of 40% strength aqueous dimethylamine solution, 1.8 g (30 millimoles) of acetic acid and 0.75 g (12 millimoles) of sodium cyanoborohydride for 5 hours at room temperature (conversion monitored by thin layer chromatography using SiO2 and 5:2:2 ethyl acetate/acetic acid/water). 50 ml of H2O were added, the mixture was rendered alkaline with 2N NaOH and extracted with ethyl acetate, the organic phase was washed with water, dried with Na2SO4 and purified over a silica gel column using a 4:1 methylene chloride/methanol mixture, and the crystalline residue from the product-containing fractions was recrystallized from ethyl acetate/petroleum ether. 1.4 g of 6-[p-(3-dimethylaminomethylpyrrol-1-yl)-phenyl]-4, 5-dihydro-5-methylpyridazin-3-one of melting point 167°-168° C. were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04710496 |
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| Source dataset | uspto-grants-1987_12 |
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| ORD ID | ord-93bd8ca7de2f428e9564a42b092cc1f5 |
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| Source note | uspto-grants-1987_12 |
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