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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856862Generated: November 2, 2026

3-Pyridinemethanol → HCID 18727250, compound

https://huagongshe.com/reaction/1856862

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-PyridinemethanolHCID 7510—
ReactantTributylphosphineHCID 13831—
ReactantHCID 18727236HCID 18727236—
SolventBenzeneHCID 241—
ProductHCID 18727250HCID 1872725041%

Reaction Steps

Tri-n-butylphosphine (0.37 ml, 1.5 mmol) was added to a solution of methyl 2-(R)-{[4-(4-bromophenyl)piperidine-1-sulfonyl]amino}-3-methylbutyrate (560 mg, 1.25 mmol), 3-pyridylcarbinol (0.15 ml, 1.5 mmol), and 1,1'-(azodicarbonyl)piperidine (377 mg, 1.5 mmol) in benzene (30 ml). After stirring at RT for 48 h, the reaction mixture was concentrated and the residue was triturated with ether (60 ml). After filtering off the solids, the ether layer was concentrated in vacuo and the residue was chromatographed (SiO2, 40% ethyl acetate/hexane) to give methyl 2-(R)-{(pyridin-3-ylmethyl)-[4-(4-bromophenyl)piperidine-1-sulfonyl]amino}-3-methylbutyrate as a colorless oil (41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06143744
Source datasetuspto-grants-2000_11
ORD IDord-be8b6eb282994dbd93857e0a8f72d49e
Source noteuspto-grants-2000_11