HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712428Generated: October 30, 2026
(2-Methoxyethyl)(methyl)amine → tert-Butyl 4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}-3-{3-[(2-methoxyethyl)methylcarbamoyl]-4-methylbenzyloxy}piperidine-1-carboxylate
https://huagongshe.com/reaction/1712428
Participants
| Role | Name | HCID | Charge |
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| Reactant | (2-Methoxyethyl)(methyl)amine | HCID 300977 | — |
| Reactant | HCID 86610009 | HCID 86610009 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | tert-Butyl 4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}-3-{3-[(2-methoxyethyl)methylcarbamoyl]-4-methylbenzyloxy}piperidine-1-carboxylate | HCID 68503252 | — |
Reaction Steps
The solution of 0.222 g of tert-butyl 3-(3-chlorocarbonyl-4-methylbenzyloxy)-4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}piperidine-1-carboxylate in 6 ml of toluene is admixed at 0° C. with the solution of 0.129 g of 2-methoxy-N-methylethylamine in 6 ml of toluene. The reaction mixture is stirred at 0° C. over a further 1 hour and then concentrated by evaporation. The title compound is obtained as a colourless oil from the residue by means of flash chromatography (SiO2 60F). Rf=0.12 (1:2 EtOAc-heptane); Rt=5.72.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07790715B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-f41f9a129e954003a1d5770efd65bc32 |
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| Source note | uspto-grants-2010_09 |
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