HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 10-[(2RS)-1-(1-pyrrolidinyl)-2-propyl]-2-phenothiazinecarbonyl chloride hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 10-[1-(1-Pyrrolidinyl)-2-propyl]-2-phenothiazinecarboxylic acid hydrochloride | HCID 14536640 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 10-[(2RS)-1-(1-pyrrolidinyl)-2-propyl]-2-phenothiazinecarbonyl chloride hydrochloride | HCID 20074886 | — |
Reaction Steps
Thionyl chloride (12.7 cc) is added in the course of 5 minutes, with stirring at a temperature of 4° C., to a suspension of 10-[(2RS)-1-(1-pyrrolidinyl)-2-propyl]-2-phenothiazinecarboxylic acid hydrochloride (9.77 g) in methylene chloride (250 cc), and stirring is continued for 90 minutes at a temperature of 20° C. The clear yellow solution obtained is concentrated to dryness under reduced pressure (30 mm Hg; 4 kPa) at 40° C. and dried to constant weight under reduced pressure (5 mm Hg; 0.67 kPa) at 50° C. to give 10-[(2RS)-1-(1-pyrrolidinyl)-2-propyl]-2-phenothiazinecarbonyl chloride hydrochloride (10.2 g) in the form of a yellow paste.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04985419 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-33461cce50594bfeb189316c444767a2 |
| Source note | uspto-grants-1991_01 |