Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 13051480 | HCID 13051480 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 20426898 | HCID 20426898 | 93% |
Reaction Steps
To 5.0 g. of 4-(4-chlorophenyl)-5H-pyrido[3,4-b][1,4]benzothiazin-3-(2H)-one (15.3 mmol.) in 50 ml. of dimethylformamide was added 30 ml. of a 5% sodium hydroxide solution (37.5 mmol.), and the resulting suspension was heated on a steam bath until a solution formed. To the solution was then added 50 ml. of a 36% formaldehyde solution (60.0 mmol.), and the resulting reaction mixture was heated until a yellow precipitate formed. The hot reaction mixture was filtered, and the precipitate was washed well with water and dried under high vacuum at room temperature to yield 4-(4-chlorophenyl)-2-(hydroxymethyl)-5H-pyrido[3,4-b][1,4]benzothiazin-3(2H)-one complexed with water (4:1) as a yellow powder (5.15 g.; 93% yield) having the structural formula, ##STR9## a melting point of greater than 300° C. and the following elemental analysis:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04500708 |
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| Source dataset | uspto-grants-1985_02 |
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| ORD ID | ord-8369cc3a223b42048d98d97bc7c7c9d8 |
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| Source note | uspto-grants-1985_02 |
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