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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181126Generated: November 1, 2026

Methanesulfonamide → HCID 72613065, compound

https://huagongshe.com/reaction/2181126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonamideHCID 72879—
ReactantHCID 73855569HCID 73855569—
ProductHCID 72613065HCID 7261306568%

Reaction Steps

Reaction of 2-(2,2-dimethyl-5-oxo-[1,3]dioxolan-4-ylidene)-N-(3-fluoro-4-methyl-benzyl)-N-methoxy-acetamide (0.135 g, 0.418 mmol) with methanesulfonamide (0.042 g, 0.44 mmol) as described in the preparation of compound 22 gave 0.102 g (68% yield) of the title amide as a white solid. 1H NMR (400 MHz, DMSO) δ: mixture of rotamers: 2.2 (3H, s, CH3), 2.87 and 2.88 (3H, 2 S, SO2CH3), 3.63 and 3.67 (3H, 2 s, OCH3), 4.73 and 4.78 (2H, 2 s, NCH2), 6.14 and 6.16 (1H, 2 s, CH), 7.04-7.27 (3H, m, aromatics). HRMS (ESI/neg) calculated for C14H16FN2O6S: [M−H]−: 359.071312; found: 359.071347.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06890942B2
Source datasetuspto-grants-2005_05
ORD IDord-be4174bc4987406183d9a26bac0de350
Source noteuspto-grants-2005_05