Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104338Generated: October 30, 2026

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

https://huagongshe.com/reaction/2104338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidin-4-olHCID 79341—
ReactantN-Boc-N-methyl-D-phenylalanineHCID 7015127—
Reactant(2E)-5-(tert-Butyloxycarbonylamino)-5-methylhex-2-enoic acidHCID 10847814—
ReactantN-Boc-N-methyl-3-(biphenyl-4-yl)-D-alanineHCID 20694694—
Product(2E)-5-Amino-5-methylhex-2-enoic acid N-((1R)-1-{N-[(1R)-1-benzyl-2-(4-hydroxypiperidin-1-yl)-2-oxoethyl]-N-methylcarbamoyl}-2-(biphenyl-4-yl)ethyl)-N-methylamideHCID 9852120—

Reaction Steps

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576062B2
Source datasetuspto-grants-2009_08
ORD IDord-01af8e5a1ffa486282414c44f2f990cf
Source noteuspto-grants-2009_08