HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536512Generated: October 25, 2026
Salicylaldehyde oxime → HCID 71285656, compound
https://huagongshe.com/reaction/536512
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Salicylaldehyde oxime | HCID 7200 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-[1-(2-Fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-4-iodo-5,5-dimethyl-5,7-dihydro-6H-pyrrolo[2,3-d]pyrimidin-6-one | HCID 86705367 | — |
| Reactant | HCID 178517712 | HCID 178517712 | — |
| Catalyst | HCID 178419072 | HCID 178419072 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 71285656 | HCID 71285656 | — |
Reaction Steps
Under argon atmosphere, 200 mg (purity 62%, 0.24 mmol) of 2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-4-iodo-5,5-dimethyl-5,7-dihydro-6H-pyrrolo[2,3-d]pyrimidin-6-one (example 15A) was suspended in 2.5 ml of absolute acetonitrile, and 545 mg (4.82 mmol) of 3-fluoropyridin-2-ol, 157 mg (0.48 mmol) of caesium carbonate, 7 mg (0.05 mmol) of copper(I) oxide and 20 mg (0.15 mmol) of 2-hydroxybenzaldehyde-oxime were added. The mixture was heated in the microwave for 1 h at 200° C. The reaction solution was filtered and purified by preparative HPLC (eluent: acetonitrile/water, gradient 20:80→100:0). 20 mg (23% of theor.) of the target compound was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859569B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-2132a30cce6547c5be1306b02eed39b8 |
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| Source note | uspto-grants-2014_10 |
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