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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896936Generated: October 25, 2026

Piperidin-4-ol → (2E)-5-Amino-5-methylhex-2-enoic acid N-((1R)-1-{N-[(1R)-1-(4-fluorobenzyl)-2-(4-hydroxypiperidin-1-yl)-2-oxoethyl]-N-methylcarbamoyl}-2-(2-naphthyl)ethyl)-N-methylamide

https://huagongshe.com/reaction/896936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidin-4-olHCID 79341—
Reactant(2R)-2-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]-3-naphthalen-2-ylpropanoic acidHCID 10065151—
Reactant(2E)-5-(tert-Butyloxycarbonylamino)-5-methylhex-2-enoic acidHCID 10847814—
ReactantN-Boc-N-methyl-4-fluoro-D-phenylalanineHCID 53833009—
Product(2E)-5-Amino-5-methylhex-2-enoic acid N-((1R)-1-{N-[(1R)-1-(4-fluorobenzyl)-2-(4-hydroxypiperidin-1-yl)-2-oxoethyl]-N-methylcarbamoyl}-2-(2-naphthyl)ethyl)-N-methylamideHCID 9960628—

Reaction Steps

This compound was prepared as in example 1 but using 4-hydroxypiperidine, (2R)-2-(N-tert-butoxycarbonyl-N-methylamino)-3-(4-fluorophenyl)propionic acid and (2R)-2-(N-tert-butoxycarbonyl-N-methylamino)-3-(2-naphthyl)propionic acid and (2E)-5-tert-butoxycarbonylamino-5-methylhex-2-enoic acid as starting materials.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06919315B1
Source datasetuspto-grants-2005_07
ORD IDord-430e9fdc26ab4417b288b725ae030872
Source noteuspto-grants-2005_07