HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742285Generated: October 30, 2026
Ethyl bromoacetate → HCID 54051188, compound
https://huagongshe.com/reaction/1742285
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 19008993 | HCID 19008993 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54051188 | HCID 54051188 | — |
Reaction Steps
To an ice-cooled solution of 3-[2-(2-aminoethyl)-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]-pyridine (1.5 g), triethylamine (1.5 ml), and N,N-dimethylformamide (15 ml) was added ethyl 2-bromoacetate (0.60 ml), and the mixture was stirred for 1 hour at room temperature. The reaction mixture was concentrated, and the residue was partitioned between chloroform and water. The organic layer was separated, washed with sodium chloride aqueous solution, dried over anhydrous magnesium sulfate, and concentrated. Purification of the residue by column chromatography on silica gel (gradient elution, using 50:1 and 25:1 mixture of chloroform and methanol) gave 3-[2-{2-(ethoxycarbonylmethylamino)ethyl}-3-oxo-2,3-dihydropyridazin-6-yl]-2-phenylpyrazolo[1,5-a]pyridine (0.90 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05338743 |
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| Source dataset | uspto-grants-1994_08 |
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| ORD ID | ord-c688cb6bc6de441281536e7b975de3cf |
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| Source note | uspto-grants-1994_08 |
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