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
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 10627240 | HCID 10627240 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | Hexanamide, 3,6-diamino-N-(2-aminoethyl)-, (R)- | HCID 3001582 | 98.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05849797 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-4eaf32e6ecdf45e6b5aad3ff5772ceb6 |
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| Source note | uspto-grants-1998_12 |
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