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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760792Generated: October 31, 2026

HCID 18337569, compound → HCID 18337576, compound

https://huagongshe.com/reaction/1760792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18337569HCID 18337569—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuran ethanolHCID 21873804—
ProductHCID 18337576HCID 1833757697.6%

Reaction Steps

To a solution of N-benzyloxy-2(R)-[(3,4-methylenedioxybenzyl)-(4-methoxy-2,6-dimethylbenzenesulfonyl)amino]-3-hydroxypropionamide (3.0 g, 5.39 mmol) in argon deoxygenated 80% ethanol-tetrahydrofuran (160 mL) was added 10% Pd—C (1.3 g), and the resulting mixture was hydrogenated at atmospheric pressure for 45 min. The reaction mixture was degassed under argon and the slurry was filtered over Celite. The Celite cake was washed with ample 80% ethanol-methylene chloride and the filtrate was concentrated to almost dryness forcing the mixture to crystallize. The slurry was filtered, washing with 50% diethyl ether-hexanes to afford N-hydroxy-2(R)-[(3,4-methylenedioxybenzyl)-(4-methoxy-2,6-dimethylbenzenesulfonyl)amino]-3-hydroxypropionamide (2.38 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06844366B2
Source datasetuspto-grants-2005_01
ORD IDord-63bf38f0583e425b81fc61a9de806930
Source noteuspto-grants-2005_01