HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 1-Methyl-1-[2-(2-propylcarbamoyl-10-phenothiazinyl)propyl]pyrrolidinium iodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | N-propyl-10-[1-(1-pyrrolidinyl)-2-propyl]-2-phenothiazinecarboxamide | HCID 9800851 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-Methyl-1-[2-(2-propylcarbamoyl-10-phenothiazinyl)propyl]pyrrolidinium iodide | HCID 19020544 | — |
Reaction Steps
A solution of N-propyl-10-[1-(1-pyrrolidinyl)-2-propyl]-2-phenothiazinecarboxamide, L series (1.1 g), and methyl iodide (0.75 cc) in acetone (40 cc) is stirred for 2 days at a temperature in the region of 20° C. The pale yellow solution thereby obtained is concentrated to dryness under reduced pressure (30 mm Hg; 4 kPa) at 40° C. and the light cream-colored meringue-like residue is suspended with stirring for 30 minutes in diethyl ether (50 cc), drained, washed with diethyl ether (3×10 cc) and dried at 40° C. under reduced pressure (5 mm Hg; 0.7 kPa). 1-Methyl-1-[2-(2-propylcarbamoyl-10-phenothiazinyl)propyl]pyrrolidinium iodide, L series (1.2 g), is thereby obtained in the form of a light beige solid, m.p. 155°-160° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05321026 |
| Source dataset | uspto-grants-1994_06 |
| ORD ID | ord-af866dc660794bae96545a023c818d6a |
| Source note | uspto-grants-1994_06 |