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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778059Generated: November 2, 2026

1,1'-Carbonyl-di-(1,2,4-triazole) → HCID 118036313, compound

https://huagongshe.com/reaction/1778059

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-Carbonyl-di-(1,2,4-triazole)HCID 4393961—
ReactantHCID 118036345HCID 118036345—
Reactant6-Amino-4-((2-methoxyethyl)amino)nicotinonitrileHCID 118036951—
SolventDimethylformamideHCID 6228—
ProductHCID 118036313HCID 118036313—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 6-amino-4-((2-methoxyethyl)amino)nicotinonitrile (intermediate 75, 81 mg, 0.422 mmol) in anhydrous DMF (0.5 ml) was added drop wise to a mixture of di(1H-1,2,4-triazol-1-yl)methanone (77 mg, 0.422 mmol) and DMF (0.5 ml) cooled at 0° C. After stirring for 2 h at 0° C. a solution of (racemic) 1-(2-(dimethoxymethyl)-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)-3-methylpyrrolidin-2-one (intermediate 331, 68 mg, 0.212 mmol) in DMF (0.5 ml) was added. The suspension was allowed to warm to room temperature, was continued to stir for 21 h and quenched by the addition of MeOH. The reaction mixture was diluted with EtOAc, phases were separated and the water phase was extracted with EtOAc. The combined organic phases were washed with water and brine, dried using Na2SO4, filtered and evaporated. The crude product was purified by silica gel column chromatography eluting with a gradient of MeOH (0-5%) in DCM. Fractions containing the product were combined, concentrated and dried to yield the title compound as a colorless residue. (UPLC-MS 3) tR 0.96 min, ESI-MS 524.4 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266883B2
Source datasetuspto-grants-2016_02
ORD IDord-de0ff769fd9b4630b4b568fb13ce0969
Source noteuspto-grants-2016_02