HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760792Generated: October 31, 2026
HCID 18337569, compound → HCID 18337576, compound
https://huagongshe.com/reaction/1760792
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 18337569 | HCID 18337569 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Tetrahydrofuran ethanol | HCID 21873804 | — |
| Product | HCID 18337576 | HCID 18337576 | 97.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06844366B2 |
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| Source dataset | uspto-grants-2005_01 |
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| ORD ID | ord-63bf38f0583e425b81fc61a9de806930 |
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| Source note | uspto-grants-2005_01 |
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