HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292029Generated: November 1, 2026
HCID 13518417, compound → 2H-1,4-Thiazin-3(4H)-one, 5-methyl-6-(4-pyridinyl)-
https://huagongshe.com/reaction/2292029
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 13518417 | HCID 13518417 | — |
| Reactant | Chloroform methanol | HCID 21584188 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | 2H-1,4-Thiazin-3(4H)-one, 5-methyl-6-(4-pyridinyl)- | HCID 3062532 | 37.1% |
Reaction Steps
Zinc powder (1.7 g) was added to a solution of 5-methyl-6-[1-(2,2,2-trichloroethoxycarbonyl)-1,4-dihydro-4-pyridinyl]-2H-1,4-thiazin-3(4H)-one (1g) in formic acid (14 ml) and the mixture was stirred at ambient temperature for 3 hours. The mixture was filtered and the filtrate was evaporated to dryness. The residue was dissolved in water (30 ml), was adjusted to pH 7.0 by 1N aqueous sodium hydroxide, was extracted with chloroform and was dried over magnesium sulfate. Chloroform was removed and the residue was purified by the preparative thin layer chromatography [Merck TLC plate, silica gel 60F254 (supplied by Merck & Co. Inc., U.S.A.), 20×20 cm, thickness=1 mm, developing solvent; chloroform/methanol=20:1] to give the titled compound (0.2 g, yield 37.1%) as pale yellow plates. The physiocochemical properties were as described above.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04800201 |
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| Source dataset | uspto-grants-1989_01 |
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| ORD ID | ord-2fa0a3eeaf2d45cfb80677ca47177c8c |
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| Source note | uspto-grants-1989_01 |
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