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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242196Generated: October 30, 2026

Methanesulfonamide → HCID 47269479, compound

https://huagongshe.com/reaction/2242196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonamideHCID 72879—
Reactant3-(Methoxycarbonyl)benzoic acidHCID 601880—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 47269479HCID 47269479—

Reaction Steps

To a mixture of isophthalic acid monomethyl ester (500.0 mg, 2.8 mmol), methanesulfonamide (340 mg, 3.6 mmol) and DMAP (440 mg, 3.6 mmol) in anhydrous dichloromethane (30 mL) was added 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (690 mg, 3.6 mmol). The mixture was allowed to stir for 12 hours at room temperature and then concentrated under reduced pressure. The residue was chromatographed on a Biotage 40M eluting with 2% methanol/98% dichloromethane to provide the titled compound. MS (EST) m/e 259 (M+H)+, 257 (M−H)−; 1H NMR (300 MHz, CD3OD) δ ppm 3.36 (s, 3 H) 3.95 (s, 3 H) 7.64 (t, J=7.80 Hz, 1 H) 8.13 (dd, J=7.80, 1.36 Hz, 1 H) 8.25 (m, 1 H) 8.55 (m, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07671076B2
Source datasetuspto-grants-2010_03
ORD IDord-afa1952d0b1a4d46918c10f56fd19df5
Source noteuspto-grants-2010_03