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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896938Generated: October 30, 2026

Piperidin-4-ol → (2E)-5-Amino-3,5-dimethylhex-2-enoic acid N-((1R)-2-(biphenyl-4-yl)-1-{N-[(1R)-2-(4-hydroxypiperidin-1-yl)-2-oxo-1-((2-thienyl)methyl)ethyl]-N-methylcarbamoyl}ethyl)-N-methylamide

https://huagongshe.com/reaction/896938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidin-4-olHCID 79341—
Reactant(2E)-5-tert-Butoxycarbonylamino-3,5-dimethylhex-2-enoic acidHCID 10753633—
ReactantN-Boc-N-methyl-3-(biphenyl-4-yl)-D-alanineHCID 20694694—
Reactant(2R)-2-(N-tert-butoxycarbonyl-N-methylamino)-3-(2-thienyl)propionic acidHCID 54365014—
Product(2E)-5-Amino-3,5-dimethylhex-2-enoic acid N-((1R)-2-(biphenyl-4-yl)-1-{N-[(1R)-2-(4-hydroxypiperidin-1-yl)-2-oxo-1-((2-thienyl)methyl)ethyl]-N-methylcarbamoyl}ethyl)-N-methylamideHCID 10952382—

Reaction Steps

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06919315B1
Source datasetuspto-grants-2005_07
ORD IDord-e0d931ba35d4401b95cccd0186fabf3e
Source noteuspto-grants-2005_07