HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930575Generated: October 31, 2026
HCID 67103617, compound → HCID 67103616, compound
https://huagongshe.com/reaction/930575
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 67103617 | HCID 67103617 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67103616 | HCID 67103616 | — |
Reaction Steps
1-[4-(4-chloro-3-methoxy-phenyl)-piperazin-1-yl]-2-(5-nitro-pyrazolo[3,4-b]pyridine-1-yl]-ethanone (15 mg) is combined with 200 mg of iron powder in 2 mL of acetic acid at 100° C. for 30 min. After cooling to rt, the reaction solution was diluted with EtOAc and filtered. The filtrate was evaporated in vacuo and purified by HPLC to provide 1-[4-(4-chloro-3-methoxy-phenyl)-piperazin-1-yl]-2-(5-amino-pyrazolo[3,4-b]pyridine-1-yl]-ethanone: HPLC retention time=1.46 minutes (Agilent Zorbax SB-C18, 2.1×50 mm, 5μ, 35° C.) using 1 ml/min flow rate, a 2.5 minute gradient of 20% to 100% B with a 1.1 minute wash at 100% B (A=0.1% formic acid/5% acetonitrile/94.9% water, B=0.1% formic acid/5% water/94.9% acetonitrile); MS (ES) M+H expect=414.2. found=415.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09296740B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-0ca0ea51f752419f9f9055ebbb276772 |
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| Source note | uspto-grants-2016_03 |
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