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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843699Generated: October 30, 2026

HCID 22612468, compound → HCID 22612485, compound

https://huagongshe.com/reaction/843699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22612468HCID 22612468—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 22612485HCID 22612485—

Reaction Steps

To a solution of N-benzyloxy-[(4-methoxybenzenesulfonyl)(2-morpholin-4-yl-2-oxoethyl)amino]acetamide (0.33 grams, 0.69 mmol) in methanol (35 mL) was added 5% palladium on activated carbon (85 mg). The mixture was agitated under 2 atmospheres hydrogen in a Parr shaker for 1.5 hours. The catalyst was removed by filtration through nylon (pore size 0.45 μm) and the solvent was evaporated. The residue was chromatorgraphed on silica gel eluting with 5% methanol in methylene chloride to afford N-methoxy-[(4-methoxybenzenesulfonyl)(2-morpholin-4-yl-2-oxoethyl)amino]acetamide as a white solid, 65 mg (24%); 1H NMR (CD3OD): δ7.82 (d, J=9.0 Hz, 2H), 7.08 (d, J=9.0 Hz, 2H), 4.24 (s, 2H), 3.88 (s, 3H), 3.84 (s, 2H), 3.68-3.64 (m, 4H), 3.58-3.50 (m, 4H); MS (thermospray): m/z 388 (M+1), 387 (M); HRMS calculated for C16H22N3O7S (M+H): 388.1178, Found 338.1180.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06380219B1
Source datasetuspto-grants-2002_04
ORD IDord-20e99661fdc142928a7822b8f153d950
Source noteuspto-grants-2002_04