Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | HCID 14502148 | HCID 14502148 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86743823 | HCID 86743823 | — |
Reaction Steps
Methyl iodide (0.036 g) is added to a solution of 10-[1-(1-pyrrolidinyl) (2RS)-2-propyl]-2-phenothiazinecarboxamidine hydrochloride (0.1 g) in dimethylformamide (1 cc) and the mixture is stirred for 16 hours at a temperature of about 20° C. The reaction solution obtained is poured into isopropyl ether (15 cc) and the oil formed is decanted, washed with isopropyl ether (15 cc) and again dissolved in a mixture of acetone and methanol (85-15 by volume) (12 cc). The preceding solution is poured dropwise, with stirring, into isopropyl ether (50 cc), and the yellow solid formed is filtered off and dried under reduced pressure (5 mm Hg; 0.67 kPa) at 50° C. 10-[1-(1-methyl-1-pyrrolidinio) (2RS)-2-propyl]-2-phenothiazinecarboxamidine iodide hydrochloride (0.11 g) is obtained in the form of a yellow powder which melts above 250° C.,
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04912105 |
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| Source dataset | uspto-grants-1990_03 |
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| ORD ID | ord-34f3502a6e054ab3be4290d0a95fc6cb |
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| Source note | uspto-grants-1990_03 |
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