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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471694Generated: October 30, 2026

Dimethylformamide → 3-((4-Formyl-6-methoxypyridin-3-yloxy)methyl)picolinonitrile

https://huagongshe.com/reaction/1471694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant5-((2-Bromopyridin-3-yl)methoxy)-2-methoxyisonicotinaldehydeHCID 71621759—
CatalystHCID 178418397HCID 178418397—
Product3-((4-Formyl-6-methoxypyridin-3-yloxy)methyl)picolinonitrileHCID 7162176084%

Reaction Conditions

Temperature125 °C

Reaction Steps

To a mixture of 5-((2-bromopyridin-3-yl)methoxy)-2-methoxyisonicotinaldehyde (100 mg, 0.31 mmol, 1 equiv), Zn (CN)2 (71 mg, 0.62 mmol, 2.0 equiv), Pd(PPh3)4 (72 mg, 0.06 mmol, 0.2 equiv) in a 5 mL microwave tube was added DMF (2 mL). The mixture was heated 15 min at 125° C. in a microwave reactor. The solid was filtered off and the filtrate was concentrated to dryness. The crude was purified on silica gel using a mixture of EtOAc and hexanes as eluent to give 3-((4-formyl-6-methoxypyridin-3-yloxy)methyl)picolinonitrile (71 mg, 84%) as a white solid. 1H NMR (400 MHz; CDCl3) δ=10.54 (s, 1H), 8.86 (d, 1H), 8.22 (s, 1H), 8.20 (d, 1H), 7.74 (dd, 1H), 6.37 (s, 1H) 5.52 (s, 2H), 4.04 (s, 3H). LRMS (M+H+) m/z 270.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012450B2
Source datasetuspto-grants-2015_04
ORD IDord-3bbeaeeeb7e44a2e81676ed8a2c1797b
Source noteuspto-grants-2015_04