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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181114Generated: October 30, 2026

Methanesulfonamide → 4-{[(3-Hydroxy-4-methanesulfonylamino-4-oxo-but-2-enoyl)-methoxy-amino]-methyl}-benzoic acid

https://huagongshe.com/reaction/2181114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonamideHCID 72879—
Reactant4-({[2-(2,2-Dimethyl-5-oxo-[1,3]dioxolan-4-ylidene)-acetyl]-methoxy-amino}-methyl)-benzoic acidHCID 73855555—
Product4-{[(3-Hydroxy-4-methanesulfonylamino-4-oxo-but-2-enoyl)-methoxy-amino]-methyl}-benzoic acidHCID 7261305895.1%

Reaction Steps

Reaction of 4-({[2-(2,2-dimethyl-5-oxo-[1,3]dioxolan-4-ylidene)-acetyl]-methoxy-amino}-methyl)-benzoic acid (0.125 g, 0.37 mmol) with methanesulfonamide (0.053 g, 0.55 mmol) as described for compound 1 gave 0.131 g (95%) of the title amide as a white solid after recrystallization from acetonitrile; mp 119-124° C. 1H NMR (400 MHz, DMSO) δ: (ppm)); mixture of rotamers: 2.99 and 3.09 (3H, 2 S, SO2CH3), 3.42 and 3.54 (3H, 2 s, OCH3), 4.63 and 4.76 (2H, 2 s, NCH2), 6.14 (1H, s, CH), 7.17 (2H, m, aromatics), 7.69 (2H, m, aromatics). HRMS (ESI/pos) calculated for C14H17N2O8S, [M+H]+: 373.070563; found: 373.070061. Anal. calcd for C14H16N2O8S: C, 45.16; H, 4.33; N, 7.52; found: C, 45.22; H, 4.70; N, 8.12.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06890942B2
Source datasetuspto-grants-2005_05
ORD IDord-2a72a62fedc342f08e1d39a9f7795dc2
Source noteuspto-grants-2005_05