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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279392Generated: October 26, 2026

Ethyl Acetate → HCID 178522278, compound

https://huagongshe.com/reaction/1279392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantRoflumilastHCID 449193—
ReactantMagnesium 2-(dioxidan-2-ide-1-carbonyl)benzoate--water (1/1/6)HCID 21894687—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 178522278HCID 17852227863.8%

Reaction Steps

A mixture of N-(3,5-Dichloropyridin-4-yl)-4-difluoromethoxy-3-cyclopropylmethoxybenzamide (3.0 g, 7.4 mmol) and magnesium monoperoxyphthalate hexahydrate (“MMPP”) (7.36 g, 14.9 mmol) in CH2Cl2/MeOH (10 mL) was stirred under reflux for 48 h. An additional amount of magnesium monoperoxyphthalate hexahydrate (7.4 g, 15 mmol) was added and the reaction mixture was stirred under reflux for an additional 24 h. Ethyl acetate was then added and the organic phase was washed by 25% aqueous NH4OAc, water and brine, dried (MgSO4) and concentrated. The residue was purified by column chromatography on silica (EtOAc) to yield N-(3.5-Dichloro-1-oxido-pyridin-4-yl)-4-difluoromethoxy-3-cyclopropylmethoxybenzamide (Compound I) as a white solid (1.98 g, 63%). 1H NMR (500 MHz, acetone-d6): δ 0.40 (m, 2H), 0.60 (m, 2H), 1.30 (m, 1H), 4.0 (d, 2H), 7.05 (t, 1H), 7.35 (d, 1H), 7.7 (m, 1H), 7.75 (s, 1H), 8.40 (s, 2H), 9.6 (bs, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448274B2
Source datasetuspto-grants-2002_09
ORD IDord-2e03889c17d84a12abaa655de8a9befb
Source noteuspto-grants-2002_09