Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366123Generated: November 4, 2026

Ammonia → 2-Ethyl-6-methylisonicotinonitrile

https://huagongshe.com/reaction/2366123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantPyridineHCID 1049—
ReactantDiisopropylethylamineHCID 81531—
ReactantPyBOPHCID 2724699—
Reactant2-Ethyl-6-methylisonicotinic acid hydrochlorideHCID 67026882—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
Product2-Ethyl-6-methylisonicotinonitrileHCID 6702700450.3%

Reaction Steps

To a solution of 2-ethyl-6-methyl-isonicotinic acid hydrochloride (1.85 g, 9.18 mmol, Example J) in DMF (90 mL), DIPEA (6.3 mL, 4.75 g, 36.7 mmol)) is added. The mixture is cooled to 0° C. before PyBOP (5.25 g, 10.1 mmol) is added. Stirring is continued at 0° C. for 15 min, then NH3 (64 mL of a 0.5 M solution in dioxane) is added. Stirring is continued for 2 h at rt before the solvent is evaporated under reduced pressure. The residue is dissolved in DCM (80 mL) and pyridine (4.5 mL, 4.39 g, 55.5 mmol) followed by TFA anhydride (6.32 mL, 9.39 g, 44.7 mmol) is added at 0° C. The mixture is stirred at rt for 2 h, before it is diluted with DCM, washed sat. aq. Na2CO3. The organic phase is dried over MgSO4, filtered and evaporated. The crude product is purified by CC on silica gel eluting with heptane:EA 4:1 to give 2-ethyl-6-methyl-isonicotinonitrile (0.675 g) as a yellow oil; 1H NMR (CDCl3): δ 1.33 (t, J=7.5 Hz, 3 H), 2.61 (s, 3 H), 2.86 (q, J=7.5 Hz, 2 H), 7.21 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697732B2
Source datasetuspto-grants-2014_04
ORD IDord-6d2b2d23b81045218aa16705351eff28
Source noteuspto-grants-2014_04