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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 76057Generated: October 29, 2026

Potassium Carbonate → {4-[4-(3-Methoxy-5-nitro-pyridin-2-yl)-phenyl]cyclohexyl}-acetic acid methyl ester

https://huagongshe.com/reaction/76057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-3-methoxy-5-nitropyridineHCID 23456152—
ReactantMethyl 2-(trans-4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclohexyl)acetateHCID 57992171—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
Product{4-[4-(3-Methoxy-5-nitro-pyridin-2-yl)-phenyl]cyclohexyl}-acetic acid methyl esterHCID 66615844—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 2-chloro-3-methoxy-5-nitro-pyridine (0.10 g, 0.53 mmol, 1.0 equiv) and {4-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-cyclohexyl}-acetic acid methyl ester (0.2 g, 0.56 mmol, 1.05 equiv) in 5 Ml DME was added 0.5 Ml saturated potassium carbonate solution and 10 mg Pd(PPh3)4 catalyst. The reaction was heated to 100° C. for 2 h. The crude reaction mixture was then concentrated in vacuo and then loaded directly onto a silica gel column. Elution with 30% EtOAc/hexanes afforded the title compound: 1H NMR (400 MHz, DMSO-d6) δ ppm 1.12-1.19 (m, 2H) 1.15 (d, J=13.14 Hz, 1H) 1.46-1.59 (m, 1H) 1.51 (dd, J=112.38, 2.78 Hz, 2H) 1.81 (d, J=5.56 Hz, 4H) 2.26 (d, J=6.82 Hz, 2H) 3.61 (s, 3H) 4.00 (s, 3H) 7.36 (d, J=8.34 Hz, 2H) 7.90 (d, J=8.34 Hz, 2H) 8.20 (d, J=2.02 Hz, 1H) 9.05 (s, 1H); (M+H)+385.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835451B2
Source datasetuspto-grants-2014_09
ORD IDord-6aaddad0bc404746b90287b4b73eb41a
Source noteuspto-grants-2014_09