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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278770Generated: October 30, 2026

Pyridine → 2-Cyclopentyl-6-methoxy-isonicotinonitrile

https://huagongshe.com/reaction/2278770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant2-Cyclopentyl-6-methoxy-isonicotinamideHCID 67491436—
SolventDichloromethaneHCID 6344—
Product2-Cyclopentyl-6-methoxy-isonicotinonitrileHCID 6749123368%

Reaction Conditions

Temperature0 °C

Reaction Steps

Pyridine (8.86 g, 91.3 mmol) is added to a solution of 2-cyclopentyl-6-methoxy-isonicotinamide (3.35 g, 15.2 mmol) in DCM (100 mL). The mixture is cooled to 0° C. before trifluoroacetic acid anhydride (9.58 g, 45.6 mmol) is added portionwise. The mixture is stirred at 0° C. for 1 h before it is diluted with DCM (100 mL) and washed with sat. aq. NaHCO3 solution (100 mL) and brine (100 mL). The separated org. phase is dried over MgSO4, filtered and concentrated. The crude product is purified by CC on silica gel eluting with heptane:EA 9:1 to give 2-cyclopentyl-6-methoxy-isonicotinonitrile (2.09 g) as a pale yellow oil; LC-MS**: tR=0.80 min, [M+1]+=not detectable; 1H NMR (D6-DMSO): δ 1.61-1.82 (m, 6H), 1.94-2.03 (m, 2H), 3.16 (quint, J=7.8 Hz, 1H), 3.89 (s, 3H), 7.15 (s, 1H), 7.28 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133179B2
Source datasetuspto-grants-2015_09
ORD IDord-37cf1f27ae884913a17d42d7a16de1fc
Source noteuspto-grants-2015_09