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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604304Generated: October 31, 2026

HCID 22612468, compound → HCID 22612485, compound

https://huagongshe.com/reaction/1604304

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 (35mL) 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 numberUS05994351
Source datasetuspto-grants-1999_11
ORD IDord-feabbf082d864241a139ede225c9498b
Source noteuspto-grants-1999_11