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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424272Generated: October 29, 2026

Dimethyl malonate → HCID 59184462, compound

https://huagongshe.com/reaction/424272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl malonateHCID 7943—
Reactant4-Amino-3-pyridinesulfonamideHCID 10975966—
ProductHCID 59184462HCID 5918446237%

Reaction Conditions

Temperature180 °C

Reaction Steps

4-amino-pyridine-3-sulfonic acid amide (0.25 g, 1.44 mmol) was suspended in malonic acid dimethyl ester (5 mL, 43.75 mmol). The flask was purged with nitrogen and the mixture was stirred at 180° C. for 60 min. Upon cooling, the mixture was diluted with ethyl acetate (5 mL) causing immediate precipitation of an undesired side product. The solid was removed by vacuum filtration and rinsed with ethyl acetate (2 mL). The filtrate was passed through a plug of silica gel, eluting with ethyl acetate followed by 5% methanol in ethyl acetate. The fractions containing the 5% methanol in ethyl acetate were combined and concentrated in vacuo to afford the desired product, (1,1-dioxo-1,4-dihydro-1λ6-pyrido[4,3-e][1,2,4]thiadiazin-3-yl)-acetic acid methyl ester (0.135 g, 0.529 mmol, 37%) as a yellow oil. LC-MS (ESI) calculated for C9H9N3O4S 255.03, found 256.0 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101800B2
Source datasetuspto-grants-2012_01
ORD IDord-f5e0ad4a80484f1394a4fbd289d536f0
Source noteuspto-grants-2012_01