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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2044100Generated: November 3, 2026

Methyl iodide → N-Methyl-N-(2-(morpholine-4-carbonyl)-5-nitrophenyl)methanesulfonamide

https://huagongshe.com/reaction/2044100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantN-(2-(Morpholine-4-carbonyl)-5-nitrophenyl)methanesulfonamideHCID 66833433—
SolventDimethylformamideHCID 6228—
ProductN-Methyl-N-(2-(morpholine-4-carbonyl)-5-nitrophenyl)methanesulfonamideHCID 6683306392%

Reaction Steps

Iodomethane (0.040 mL, 0.643 mmol) was added to a solution of N-(2-(morpholine-4-carbonyl)-5-nitrophenyl)methanesulfonamide (108 mg, 0.321 mmol) and 60% suspension of NaH (16.5 mg, 0.413 mmol) in DMF (0.5 mL) at room temperature. After 1.5 h at room temperature, the mixture was carefully quenched with water (10 mL) and extracted with EtOAc (3×4 mL). The combined EtOAc phase was concentrated, purified by silica gel chromatography, and eluted with 10-100% EtOAc in hexanes to give a yellow oil (101.3 mg, 92% yield). LCMS: (M+H)+=344.0. 1H NMR (400 MHz, DMSO-d6) δ ppm 8.39 (1H, d, J=2.26 Hz), 8.27 (1H, dd, J=8.53, 2.26 Hz), 7.71 (1H, d, J=8.53 Hz), 3.69-3.78 (2H, m), 3.47-3.61 (4H, m), 3.10-3.30 (2H, m), 3.21 (3H, s), 3.17 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586751B2
Source datasetuspto-grants-2013_11
ORD IDord-a50541fbf0954a9e8fe9e64cac97418c
Source noteuspto-grants-2013_11