HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81697Generated: October 30, 2026
Potassium Carbonate → 2-{4-Amino-2-[(3-chloro-4-methoxy-5-methylpyridin-2-yl)methyl]-2,7-dihydro-6-thia-1,2,3,5-tetraazabenzo[cd]azulen-8-yl}-N-methylacetamide
https://huagongshe.com/reaction/81697
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Chloro-2-(chloromethyl)-4-methoxy-5-methylpyridine hydrochloride | HCID 66617932 | — |
| Reactant | HCID 136403539 | HCID 136403539 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-{4-Amino-2-[(3-chloro-4-methoxy-5-methylpyridin-2-yl)methyl]-2,7-dihydro-6-thia-1,2,3,5-tetraazabenzo[cd]azulen-8-yl}-N-methylacetamide | HCID 66618074 | 84.4% |
Reaction Steps
Dimethylformamide (1 ml) was added to 2-(4-amino-2,7-dihydro-6-thia-1,2,3,5-tetraazabenzo[cd]azulen-8-yl)-N-methylacetamide trifluoroacetate (28 mg), 3-chloro-2-(chloromethyl)-4-methoxy-5-methylpyridine hydrochloride (36 mg), and potassium carbonate (69 mg). The resulting mixture was stirred at 60° C. for 2.5 hours. Thereafter, the insoluble matter was removed by filtration, and the solvent was then distilled away in a nitrogen stream. The resulting residue was dissolved in dimethyl sulfoxide (1 ml), and it was then purified by preparatory reverse-phase HPLC. The solvent was distilled away under reduced pressure, so as to obtain the title compound (27.0 mg) as a solid (amorphous substance).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846703B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-f3eeb77163c44ed98820b86697c318e4 |
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| Source note | uspto-grants-2014_09 |
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