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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422399Generated: October 26, 2026

Dimethylformamide dimethyl acetal → HCID 178423428, compound

https://huagongshe.com/reaction/1422399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamide dimethyl acetalHCID 78373—
ReactantHydrazine, acetate (1:1)HCID 165591—
Reactant2-Chloro-6-methylpyridine-4-carboxamideHCID 59534429—
SolventAcetic AcidHCID 176—
SolventDimethylformamideHCID 6228—
ProductHCID 178423428HCID 178423428—

Reaction Conditions

Temperature90 °C

Reaction Steps

2-Chloro-6-methyl-isonicotinamide (1.23 g) and N,N-dimethylformamide dimethyl acetal (1.05 ml) were dissolved in dry DMF (4 ml) under inert atmosphere and the resulting solution was heated to 90° C. and stirred for 1 h. The reaction mixture was cooled to room temperature and a solution of hydrazine acetate (3.32 g) in acetic acid (8 ml) was dropwise added. The mixture was heated to 90° C. and stirred for 1 h. The solvent was removed under reduced pressure and the residue partitioned between saturated aqueous solution of NaHCO3 and EtOAc. The organic phase was separated, washed with brine, dried under Na2SO4, filtered and the solvent was evaporated under reduced pressure. The crude was purified by flash column chromatography (10 g Isolute® silica gel cartridge; gradient elution: hexane/EtOAc from 1/1 to 3/7) affording 2-Chloro-6-methyl-4-(1H-[1,2,4]triazol-3-yl)-pyridine (0.92 g). GC (Rt)=13.21 min (method=3A)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE045323E1
Source datasetuspto-grants-2015_01
ORD IDord-55f536309d184399ab5d5661a44892f3
Source noteuspto-grants-2015_01