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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424181Generated: October 30, 2026

Methyl malonyl chloride → n-(4-Methanesulfonylamino-2-sulfamoylphenyl)malonamic acid methyl ester

https://huagongshe.com/reaction/424181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl malonyl chlorideHCID 123460—
Reactant2-Amino-5-[(methylsulfonyl)amino]benzenesulfonamideHCID 24950657—
SolventTetrahydrofuranHCID 8028—
Productn-(4-Methanesulfonylamino-2-sulfamoylphenyl)malonamic acid methyl esterHCID 2485839972%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Amino-5-methanesulfonylamino-benzenesulfonamide (prepared as described in Example 1d, 1.70 kg, 6.40 mol) was dissolved in tetrahydrofuran (35 L), and was then cooled to 0° C. Methyl 3-chloro-3-oxopropionate (792 mL, 7.40 mol) was added slowly, and the resulting mixture was then allowed to warm to 23° C. and stirred for 2 days. The solvent was removed in vacuo, and the residue was then diluted with water (4 L) and saturated aqueous sodium bicarbonate solution (2 L). The resulting solid was filtered, and was then washed with water (5 L). The solid was suspended in hot methanol (15 mL/g), and was then cooled to 23° C. and filtered to afford the desired product, N-(4-methanesulfonylamino-2-sulfamoyl-phenyl)-malonamic acid methyl ester (1.68 kg, 4.61 mol, 72%), as a brown solid. 1H NMR (400 MHz, DMSO-d6) δ: 3.02 (3H, s), 3.60 (2H, s), 3.66 (3H, s), 7.38 (1H, dd, J1=2.3 Hz, J2=8.6 Hz), 7.53 (2H, bs), 7.73 (1H, d, J=2.4 Hz), 7.83 (1H, d, J=8.7 Hz), 9.43 (1H, s), 9.99 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101800B2
Source datasetuspto-grants-2012_01
ORD IDord-1b5c321f7a7d493ea0b8ec02b1b662a7
Source noteuspto-grants-2012_01