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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651815Generated: October 30, 2026

HCID 70237630, compound → HCID 70204322, compound

https://huagongshe.com/reaction/651815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 70237630HCID 70237630—
CatalystAdams' catalystHCID 345198—
SolventAcetic AcidHCID 176—
ProductHCID 70204322HCID 7020432225.5%

Reaction Steps

A solution of 0.500 g of 2(R)-[1(S)-(tert-butoxycarbonyl)-4-phenylbutyl]-4-methyl-N-(2,4,6-trioxo-1,3,5-triazin-1-yl)valeramide (prepared as described in Example 44, part (i)) in 7 ml of glacial acetic acid was hydrogenated in the presence of 0.05 g of platinum (IV) oxide for 1.5 hours. Filtration and evaporation gave a residue which was purified by flash column chromatography on silica gel using ethyl acetate/hexane (1:1) as the eluant to give 0.129 g of 2(R)-[4-cyclohexyl-1(S)-(tert-butoxycarbonyl)butyl]-N-(2,4,6-trioxo-1,3,5-triazin-1-yl)-4-methylvaleramide in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06281363B1
Source datasetuspto-grants-2001_08
ORD IDord-762ae3525baf40c295fe341fec2416fe
Source noteuspto-grants-2001_08