HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279869Generated: October 31, 2026
1,2-Ethanediamine, N1,N1,N2-trimethyl- → HCID 59909840, compound
https://huagongshe.com/reaction/1279869
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Ethanediamine, N1,N1,N2-trimethyl- | HCID 67338 | — |
| Reactant | ethyl 5-{(1R)-1-[2-(tert-butoxy)-2-oxoethyl]4-cyclohexylbutyl}-1,2,4-oxadiazole-3-carboxylate | HCID 59909797 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59909840 | HCID 59909840 | 154.1% |
Reaction Steps
A solution of ethyl 5-{(1R)-1-[2-(tert-butoxy)-2-oxoethyl]-4-cyclohexylbutyl)-1,2,4-oxadiazole-3-carboxylate (Preparation 3) (560 mg, 1.42 mmol) in ethanol (2 ml) was treated with N,N,N′-trimethylethylenediamine (900 l, 0.91 mmol) and the resulting mixture was heated at 85° C. in a sealed tube for 4.5 hours. The solvent was removed under reduced pressure and the residue was purified by column chromatography on silica gel eluting with a system of 95:5:0.5 (dichloromethane:methanol:ammonia) to afford the title compound as a colourless oil (632 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06448278B2 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-3cfd6e333d6e47f78bc58207bea966fd |
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| Source note | uspto-grants-2002_09 |
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