Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Bromoacetonitrile | HCID 11534 | — |
| Reactant | 1,2-Dimethyl-10-(3-aminopropyl)phenothiazine-5-oxide | HCID 9861144 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22742446 | HCID 22742446 | 27.6% |
Reaction Steps
2.25 g of 1,2-dimethyl-10-(3-aminopropyl)phenothiazine-5-oxide synthesized in Example 8, 990 mg of bromoacetonitrile and 1.2 g of potassium carbonate were dissolved in 50 ml of N,N-dimethylformamide followed by stirring at 80° C. for 10 min. Then the reaction mixture was cooled to room temperature and, after adding water, extracted with ethyl acetate. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. After evaporating the solvent under reduced pressure, the residue was purified by silica gel column chromatography to give 670 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06703388B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-e53e6bd860f84c7cbacd36a9742e0324 |
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| Source note | uspto-grants-2004_03 |
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