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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381341Generated: November 1, 2026

2-(Piperidin-1-yl)phenol → HCID 57919185, compound

https://huagongshe.com/reaction/2381341

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Piperidin-1-yl)phenolHCID 3262250—
Reactant4,5-Dichloro-2-(tetrahydro-pyran-2-yl)-2H-pyridazin-3-oneHCID 10729262—
ReactantMethyl 2-bromo-3-cyclopentylpropanoateHCID 57919172—
ProductHCID 57919185HCID 5791918597%

Reaction Steps

In an analogous manner to the stepwise sequence outlined in intermediate 19, starting from 4,5-dichloro-2-(tetrahydropyran-2-yl)-2H-pyridazin-3-one (Intermediate 20) and 2-(piperidin-1-yl)phenol and alkylating with 2-bromo-3-cyclopentyl-propionic acid methyl ester (Intermediate 10) afforded 3-cyclopentyl-2-[6-oxo-4-(2-piperidin-1-yl-phenoxy)-6H-pyridazin-1-yl]-propionic acid (3.3 g, 97%) as a white solid; ESI-MS 412 [M+H+]; HPLC conditions (0.17% trifluoroacetic acid in acetonitrile/water, 50%-100% acetonitrile, gradient, 1 mL/min, Venusil MP-C18, C18-15 cm×4.6 mm-5 μm), purity>98%. 1H-NMR (300 MHz, CDCl3) δ 7.78 (s, 1H), 7.08 (m, 4H), 5.99 (s, 1H), 5.52 (m, 1H), 2.93 (m, 4H), 2.35 (m, 1H), 2.12 (m, 1H), 1.60 (m, 13H), 1.16 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258134B2
Source datasetuspto-grants-2012_09
ORD IDord-bdcc0b6a11b64a1dacdcf86da22517eb
Source noteuspto-grants-2012_09