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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842990Generated: October 31, 2026

3-Pyridinemethanol → HCID 18727250, compound

https://huagongshe.com/reaction/842990

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 numberUS06376506B1
Source datasetuspto-grants-2002_04
ORD IDord-f0f1bf95661147dd82519e1fa4354866
Source noteuspto-grants-2002_04