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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-oxo-3,4-dihydro-2H-1,4-benzothiazine-6-carboxylateHCID 699501—
SolventTetrahydrofuranHCID 8028—
Productmethyl 3,4-dihydro-2H-1,4-benzothiazine-6-carboxylateHCID 1779664796%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696200B2
Source datasetuspto-grants-2010_04
ORD IDord-174708bb10dc4ea984c2b8663f64ef1a
Source noteuspto-grants-2010_04