Hydrochloric Acid → Quinoxalin-6-ylboronic acid

To 6-quinoxaline boronic acid pinacol ester (S50) (256 mg, 1.00 mmol, 1.00 equiv) in THF (2.0 mL) at 23° C. was added H2O (8.0 mL) and NaIO4 (321 mg, 1.50 mmol, 1.50 equiv). After stirring for 1.0 hr at 23° C., the reaction mixture was added to 1N HCl aq (20 mL) and was further stirred for 1.0 hr. To the reaction mixture was added EtOAc (20 mL) and the phases were separated. The aqueous phase was extracted with EtOAc (2×20 mL). The combined organic phases are washed with brine (20 mL) and dried (Na2SO4). The filtrate was concentrated in vacuo and the residue was triturated with Et2O to afford 121 mg of the title compound as a colorless solid (70% yield).

1. stirringwas further stirred for 1.0 hr
2. customthe phases were separated
3. extractionThe aqueous phase was extracted with EtOAc (2×20 mL)
4. washThe combined organic phases are washed with brine (20 mL)
5. dry with materialdried (Na2SO4)
6. concentrationThe filtrate was concentrated in vacuo
7. customthe residue was triturated with Et2O

ORD 기록

ord-f8c6885228864c989c953c677f519d3e

출처 데이터셋

uspto-grants-2015_05

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US09024093B2