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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1692401Generated: October 31, 2026

4-(1-Pyrrolidinyl)piperidine → HCID 57580543, compound

https://huagongshe.com/reaction/1692401

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(1-Pyrrolidinyl)piperidineHCID 78703—
Reactant3-(Trifluoromethoxy)phenylboronic Acid (contains varying amounts of Anhydride)HCID 2734385—
Reactant3-bromo-2,6-dimethylbenzoic acidHCID 8167142—
ProductHCID 57580543HCID 57580543—

Reaction Steps

In analogy to the procedure described for intermediate 1,2,4-dimethyl-3′-trifluoromethoxy-biphenyl-3-carboxylic acid (prepared from 3-bromo-2,6-dimethyl-benzoic acid [Lee, J.; et al. Bioorganic & Medicinal Chemistry Letters (2003), 13(11), 1879-1882] and 3-trifluoromethoxy-phenyl boronic acid in analogy to the procedure described for the preparation of example 1) was converted into its acid chloride and reacted with 4-pyrrolidin-1-yl-piperidine to give the title compound as light yellow solid. MS: 447.3 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153805B2
Source datasetuspto-grants-2012_04
ORD IDord-c049e1ee654a4e6fb94adc51d6ba8cdb
Source noteuspto-grants-2012_04