Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778030Generated: November 1, 2026

1,1'-Carbonyl-di-(1,2,4-triazole) → HCID 118036489, compound

https://huagongshe.com/reaction/1778030

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-Carbonyl-di-(1,2,4-triazole)HCID 4393961—
Reactant6-Amino-4-(bicyclo[1.1.1]pentan-1-ylamino)nicotinonitrileHCID 118036201—
Reactant1-((2-(Dimethoxymethyl)-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)methyl)-4-methylpiperazin-2-oneHCID 118036658—
SolventDimethylformamideHCID 6228—
ProductHCID 118036489HCID 118036489—

Reaction Steps

A solution of 6-amino-4-(bicyclo[1.1.1]pentan-1-ylamino)nicotinonitrile (intermediate 277, 61 mg, 0.305 mmol) in anhydrous DMF (1.5 ml) was added to a solution of di(1H-1,2,4-triazol-1-yl)methanone (50 mg, 0.305 mmol) in DMF (1.5 ml) at 0° C. After stirring for 1.5 h at room temperature a solution of 1-((2-(dimethoxymethyl)-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)methyl)-4-methylpiperazin-2-one (intermediate 81, 60 mg, 0.179 mmol) in DMF (1.5 ml) was added. The reaction mixture was stirred for 18 h at room temperature, then evaporated directly onto isolate and purified by normal phase chromatography: 12 g RediSep® silica column; eluting with EtOAc then a gradient from DCM to 10% MeOH in DCM. Product containing fractions were combined and evaporated to give the title compound as a yellow solid. (UPLC-MS 6) tR 1.00; ESI-MS 561.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266883B2
Source datasetuspto-grants-2016_02
ORD IDord-5e52f2b7bfc848b29eabd3fb695c41f6
Source noteuspto-grants-2016_02