HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641325Generated: October 25, 2026
Methyl 3-oxo-3,4-dihydro-2H-1,4-benzothiazine-6-carboxylate → methyl 3,4-dihydro-2H-1,4-benzothiazine-6-carboxylate
https://huagongshe.com/reaction/641325
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 3-oxo-3,4-dihydro-2H-1,4-benzothiazine-6-carboxylate | HCID 699501 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | methyl 3,4-dihydro-2H-1,4-benzothiazine-6-carboxylate | HCID 17796647 | 96% |
Reaction Steps
Borane-tetrahydrofuran complex solution (1 M in tetrahydrofuran, 45 mL, 45 mmol) was added at 0° C. to a suspension of methyl-3-oxo-3,4-dihydro-2H-1,4-benzothiazine-6-carboxylate (2.00 g, 8.96 mmol) in tetrahydrofuran (20 mL). The ice bath was removed, the homogenous solution stirred at room temperature for 2 h, then excess reagent was destroyed by careful addition of methanol (42 mL) at 0° C. After evaporation of volatile material, the residue was taken up in 5% methanolic sulfuric acid solution (25 mL) and the solution was heated at reflux over 80 min. After cooling, the reaction mixture was partitioned between ethyl acetate and water, the organic layer was dried (MgSO4) and evaporated to produce 3,4-dihydro-2H-benzo[1,4]thiazine-6-carboxylic acid methyl ester (1.79 g, 96%). Light yellow solid, MS (ISP)=210.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07696200B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-174708bb10dc4ea984c2b8663f64ef1a |
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| Source note | uspto-grants-2010_04 |
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