HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromoethanol → 2-(2-Hydroxyethyl)-10-trifluoromethyl-1H-pyrimido[5,4,3-kl]phenothiazine-1,3(2H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 10-Trifluoromethyl-1H-pyrimido[5,4,3-kl]phenothiazine-1,3-(2H)-dione | HCID 12223715 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(2-Hydroxyethyl)-10-trifluoromethyl-1H-pyrimido[5,4,3-kl]phenothiazine-1,3(2H)-dione | HCID 12223717 | — |
Reaction Steps
57% Sodium hydride in mineral oil (8.4 g., 0.200 mol.) was added to a stirred solution of 28.0 g (0.0834 mol.) of 10-trifluoromethyl-1H-pyrimido[5,4,3-kl]phenothiazine -1,3(2H)-dione in 220 ml. of dry dimethylformamide. The mixture was stirred for 1 hour at 25°, then 54.0 g. (0.432 mol.) of 2-bromoethanol was added. The resulting mixture was stirred for 4.5 hours at 25°, then filtered. The filtrate was evaporated to dryness under reduced pressure and the residue was chromatographed on silica gel with chloroform and 90% chloroform-methanol as eluants to give the title compound, m.p. 90°-93° (methanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03962438 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-abfdd56c44524c78aee8c0fd7e702b5a |
| Source note | uspto-grants-1976_06 |