HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892387Generated: October 31, 2026
Ethanol, 2-(aminooxy)- → HCID 50991634, compound
https://huagongshe.com/reaction/1892387
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol, 2-(aminooxy)- | HCID 3014186 | — |
| Reactant | 1-(3-(Difluoro(quinolin-6-yl)methyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)ethanone | HCID 58190468 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 50991634 | HCID 50991634 | 55.3% |
Reaction Steps
A solution of 1-(3-(difluoro(quinolin-6-yl)methyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)ethanone (54 mg, 0.159 mmol) and 2-(aminooxy)ethanol (intermediate S) (36.1 mg, 0.318 mmol) in 8 mL of MeOH was stirred at it overnight. Solvent was evaporated and the residue was partitioned between water and EtOAc. Aqueous layer was extracted with EtOAc twice. Organic layers were combined, washed with brine and dried over Na2SO4. Solvent was evaporated and the crude was purified by HPLC (basic with 0.05% NH4OH) to give 35 mg (55%) of the title compound as a white solid. 1H-NMR (400 MHz, MeOH-d4) δ ppm 8.98 (d, 1H), 8.52 (d, 1H), 8.43 (s, 1H), 8.23 (d, 1H), 8.19 (d, 1H), 8.06 (d, 1H), 8.04 (d, 1H), 7.66 (m, 1H), 4.36 (m, 2H), 3.84 (m, 2H), 2.18 (s, 3H). LCMS (method B): [MH]+=398.9, tR=2.29 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507676B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-83462306c9be47ffba1b74e5f376ebf1 |
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| Source note | uspto-grants-2013_08 |
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