Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 20426913 | HCID 20426913 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 20426902 | HCID 20426902 | 94% |
Reaction Steps
To 1.0 g. of 7-trifluoromethyl-4-(4-chlorophenyl)-5H-pyrido[3,4-b][1,4]benzothiazin-3(2H)-one (2.5 mmol.) in 10 ml. dimethylformamide was added 6.0 ml. of a 5% sodium hydroxide solution (7.5 mmol.), and the resulting suspension was heated on a steam bath until a solution formed. To the solution was then added 10 ml. of a 36% formaldehyde solution (12.0 mmol.), and the resulting reaction mixture was heated until a yellow precipitate formed. The hot reaction mixture was filtered, and the precipitate was washed with water and dried under high vacuum at room temperature to yield 7-trifluoromethyl-4-(4-chlorophenyl)-2-(hydroxymethyl)-5H-pyrido[3,4-b][1,4]benzothiazin-3(2H)-one as a yellow powder (1.0 g.; 94% yield) having the structural formula, ##STR24## a melting point of 204° C. (with decomposition) and the following elemental analysis:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04500708 |
|---|
| Source dataset | uspto-grants-1985_02 |
|---|
| ORD ID | ord-fc0b0ef3591d48d8b76335ca7e2f3747 |
|---|
| Source note | uspto-grants-1985_02 |
|---|