Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360294Generated: 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/1360294

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 numberUS07879845B2
Source datasetuspto-grants-2011_02
ORD IDord-b49744dc1f8047058021274eec68a319
Source noteuspto-grants-2011_02