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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457951Generated: November 1, 2026

HCID 10627240, compound → Hexanamide, 3,6-diamino-N-(2-aminoethyl)-, (R)-

https://huagongshe.com/reaction/1457951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10627240HCID 10627240—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHexanamide, 3,6-diamino-N-(2-aminoethyl)-, (R)-HCID 300158298.9%

Reaction Steps

In 180 ml of methanol were suspended 1.41 g (2.39 mmol) of (R)-3,6-bis(benzyloxycarbonylamino)-N-(2-benzyloxycarbonylaminoethyl)hexanamide. To the resulting suspension was added a suspension of 718 mg of 10% palladium-carbon in 20 ml of water. After stirring, hydrogen gas was passed through the resulting mixture at room temperature for 3 hours to effect the reaction. The palladium-corbon was filtered off from the reaction mixture obtained, and the filtrate was concentrated to dryness. The residue obtained was dissolved in 15 ml of water and then subjected to a chromatography on a column of "Amberlite CG-50" (trade name, NH4+ -form, 50 ml). After the column was washed with 200 ml of water, the column was eluted with aqueous ammonia at concentrations gradiently varying from 0.5% to 4.0% (0.5%-increased steps; 200 ml at each concentration). Fractions of the eluate as eluted with 2.5% to 3.5% aqueous ammonia were combined together and concentrated to dryness, to afford 445 mg of (R)-3,6-diamino-N-(2-aminoethyl)hexanamide as a colorless paste.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849797
Source datasetuspto-grants-1998_12
ORD IDord-4eaf32e6ecdf45e6b5aad3ff5772ceb6
Source noteuspto-grants-1998_12