HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182995Generated: October 29, 2026
N-Methylbenzylamine → HCID 59909818, compound
https://huagongshe.com/reaction/2182995
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methylbenzylamine | HCID 7669 | — |
| 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 59909818 | HCID 59909818 | 82.9% |
Reaction Steps
A solution of ethyl 5-{(1R)-1-[2-(tert-butoxy)-2-oxoethyl]-4-cyclohexylbutyl}-1,2,4-oxadiazole-3-carboxylate (Preparation 3) (300 mg, 0.76 mmol) in ethanol (4 ml) was treated with N-benzyl-N-methylamine (0.98 ml, 7.60 mmol) and the resulting mixture was heated at 60° C. under a nitrogen atmosphere for 16 hours. The mixture was cooled and the solvent removed under reduced pressure. The residue was purified by column chromatography on silica gel eluting with a gradient system of dichloromethane:ethyl acetate (100:0) gradually changing to dichloromethane:ethyl acetate (95:5) to afford the title compound (296 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-f78879a7a80e498fb77319cbfb4aa626 |
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| Source note | uspto-grants-2005_05 |
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