HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410260Generated: November 1, 2026
1H-Indazole-4-boronic acid → HCID 86691498, compound
https://huagongshe.com/reaction/2410260
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1H-Indazole-4-boronic acid | HCID 44118310 | — |
| Reactant | HCID 86691499 | HCID 86691499 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 86691498 | HCID 86691498 | 31% |
Reaction Steps
Tetraisopropyl (2-(2-chloropyridin-4-yl)-1-fluoroethane-1,1-diyl)bis(phosphonate) (78 mg; 0.16 mmol), Pd(PPh3)4 (37 mg; 0.032 mmol) and (1H-indazol-4-yl)boronic acid (52 mg; 0.32 mmol) are mixed in microwave vial (2-5 mL). The vial is capped with a septum, 2.0 mL of DME is added and the reaction mixture is immediately flushed with argon. Sodium carbonate solution (0.20 mL; 2M) is added and the mixture is flushed again with argon. The vial is re-capped with Teflon cap and irradiated in microwave for 15 min at 110° C. The mixture is cooled, diluted with EtOAc and filtered through Celite™, the Celite™ is rinsed 3× with EtOAc/MeOH (1:1). The filtrates are concentrated and deposited on silica. Purification by column chromatography on silica gel (pre treated with 1% NEt3 in hexanes) using a solvent gradient from hexanes to EtOAc, and then to 50% MeOH in EtOAc lead to the isolation of the product as a yellow oil (28 mg; 31% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08816082B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-59cf6cbbab5f4f02800700d103147657 |
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| Source note | uspto-grants-2014_08 |
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