HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Aminophenylboronic acid → HCID 25213275, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Aminophenylboronic acid | HCID 92269 | — |
| Reactant | N-(6-bromo[1,2,4]triazolo[1,5-a]pyridin-2-yl)nicotinamide | HCID 25212519 | — |
| Product | HCID 25213275 | HCID 25213275 | 40% |
Reaction Steps
The title compound was prepared following procedure described for intermediate A1 step a) but starting from N-(6-bromo[1,2,4]triazolo[1,5-a]pyridin-2-yl)nicotinamide ((B6), 75 mg; 0.24 mmol; 1.0 eq.) and 3-aminobenzeneboronic acid (64 mg; 0.47 mmol; 2.0 eq.). Purification by flash chromatography on silica (MeOH/DCM, gradient from 0:100 to 10:90) gave the title compound as a dark red solid (31 mg, 40%). HPLC, Rt: 1.07 min. (purity 96.3%). LC/MS, M+(ESI): 331.4, M−(ESI): 329.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08263595B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-29ae695c9efd4fba8a5fee7185b08290 |
| Source note | uspto-grants-2012_09 |