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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1'-Carbonyl-di-(1,2,4-triazole) | HCID 4393961 | — |
| Reactant | HCID 118036345 | HCID 118036345 | — |
| Reactant | 6-Amino-4-((2-methoxyethyl)amino)nicotinonitrile | HCID 118036951 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 118036313 | HCID 118036313 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09266883B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-de0ff769fd9b4630b4b568fb13ce0969 |
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| Source note | uspto-grants-2016_02 |
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