HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219201Generated: October 25, 2026
Hydrochloric Acid → 3-(2-Methoxyethoxy)-6-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)quinoline
https://huagongshe.com/reaction/219201
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-Hydrazinyl-6-phenylpyridazine | HCID 6409842 | — |
| Reactant | Tert-butyl 2-(3-(2-methoxyethoxy)quinolin-6-yl)acetate | HCID 57690925 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(2-Methoxyethoxy)-6-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)quinoline | HCID 57691072 | — |
Reaction Steps
To a 5 ml CEM microwave tube was added tert-butyl 2-(3-(2-methoxyethoxy)quinolin-6-yl)acetate (0.080 g, 0.25 mmol), 1-(6-phenylpyridazin-3-yl)hydrazine (0.094 g, 0.50 mmol), HYDROCHLORIC ACID (0.063 ml, 0.76 mmol), and water (0.2 mL) as solvent. The vial was sealed and first heated at 90° C. for 30 min then placed into CEM microwave for 15 min. at 140° C., with 100 Watts of power via Powermax. The reaction mixture was adjusted the pH to 7 by adding 5 N NaOH and the precipitate was collected via filtration. The brown ppt. was dissolved in DCM. The organic was washed with water, dried over MgSO4, and removed solvent in vacuo. The crude product was purified using SiO2 chromatography (TELEDYNE ISCO REDISEP®, P/N 68-2203-026, 12 g SiO2, DCM:EtOAc:MeOH=60%:37%:3%, Flow=30 mL/min) to afford the desired product as light yellowish solid. MS m/z: 412.3 (M+H). Calc'd. for C24H21N5O2−411.45.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08198448B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-e02cef23401c444288496a66e9aff661 |
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| Source note | uspto-grants-2012_06 |
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