HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrrolidine → 7-chloro-10-[(2RS)-1-(1-pyrrolidinyl)-2-propyl]-2-phenothiazinecarbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | (2RS)-2-(7-chloro-2-cyano-10-phenothiazinyl)propyl methanesulphonate | HCID 15925250 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 7-chloro-10-[(2RS)-1-(1-pyrrolidinyl)-2-propyl]-2-phenothiazinecarbonitrile | HCID 15925366 | — |
Reaction Steps
Pyrrolidine (21.1 cc) is added to a suspension of (2RS)-2-(7-chloro-2-cyano-10-phenothiazinyl)propyl methanesulphonate (72.1 g) in toluene (166 cc). The mixture is brought to 120° C. for 21 hours, and then to 150° C. for 12 hours. After cooling, the mixture is washed with distilled water (5×250 cc). The organic phase is dried over magnesium sulphate, filtered and concentrated to dryness under reduced pressure (30 mm Hg; 4 kPa) to give 7-chloro-10-[(2RS)-1-(1-pyrrolidinyl)-2-propyl]-2-phenothiazinecarbonitrile (19.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04985419 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-0f644bf331754bae8253500e3e7b110c |
| Source note | uspto-grants-1991_01 |