HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239666Generated: October 26, 2026
Dichloromethane → HCID 136065805, compound
https://huagongshe.com/reaction/239666
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3,5-Dimethylpyrazole-4-boronic acid, pinacol ester | HCID 16217713 | — |
| Reactant | 2-(1-(4-amino-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl)-3-(3-fluorophenyl)-4H-chromen-4-one | HCID 66579932 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 136065805 | HCID 136065805 | 7.6% |
Reaction Steps
To a solution of Example 57c (0.350 g, 0.661 mmoles) in DMF (6 ml), ethanol (3 ml) and water (3 ml), 3,5-Dimethylpyrazole-4-boronic acid pinacol ester (0.191 g, 0.859 mmoles) and sodium carbonate (0.350 g, 3.30 mmoles) were added and the system is degassed for 30 min. Tetrakistriphenylphosphine Palladium (0.150 g, 0.130 mmoles) was added under nitrogen atmosphere and heated to 80° C. After 12 h, the reaction mixture was celite filtered, concentrated and extracted with ethyl acetate. The organic layer was dried over sodium sulphate and concentrated under reduced pressure. The crude product was purified by column chromatography with methanol: dichloromethane to afford the title compound as brown solid (0.025 g, 7% yield). MP: 240-243° C. 1H-NMR (δ ppm, DMSO-d6, 400 MHz): δ 12.44(s,1H), 8.04(dd, J=8.0,1.6 Hz, 1H), 8.01(s,1H), 7.85(s,1H), 7.61(d, J=8.3 Hz, 1H), 7.52(dt, J=7.9,0.7 Hz, 1H), 7.33(br m,1H), 7.12-6.95(m, 3H), 5.97(q, J=7.0 Hz, 1H), 2.09(s,6H), 1.86(d, J=7.0 Hz, 3H). Mass: 495.84(M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642607B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-01fecfe4e94c4652a208f9f519c03942 |
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| Source note | uspto-grants-2014_02 |
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