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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660844Generated: October 27, 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/1660844

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 numberUS08030308B2
Source datasetuspto-grants-2011_10
ORD IDord-1b4592677626440290f5d03e0eae5472
Source noteuspto-grants-2011_10