HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183043Generated: November 2, 2026
1,3-Propanediamine, N1,N1,N3-trimethyl- → HCID 59909772, compound
https://huagongshe.com/reaction/2183043
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Propanediamine, N1,N1,N3-trimethyl- | HCID 78302 | — |
| 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 59909772 | HCID 59909772 | 78.7% |
Reaction Steps
A solution of ethyl 5-{(1R)-1-[2-(tert-butoxy)-2-oxoethyl]-4-cyclohexylbutyl}-1,2,4-oxadiazole-3-carboxylate (Preparation 3) (550 mg, 1.40 mmol) in ethanol (2 ml) was treated with N,N,N′-trimethyl-1,3-propanediamine (1.02 ml, 7.00 mmol) and the resulting mixture was heated at 85° C. in a sealed tube for 3 hours. The solvent removed under reduced pressure. The residue was purified by column chromatography on silica eluting with a gradient system of 97:3:0.3 (dichloromethane:methanol:ammonia) gradually changing to 90:10:1 (dichloromethane:methanol:ammonia) to afford the title compound as a colourless oil (512 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06897306B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-ec93a86167874cfe913205617747af35 |
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| Source note | uspto-grants-2005_05 |
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