Dimethylformamide → Methyl 4-hydroxy-3-iodobenzoate

To a solution of compound 1 (200 mg, 1.077 mmol) and 2-iodopropane (322 uL, 3.23 mmol) in DMF (10 mL) was added DIEA (750 uL, 4.31 mmol). The reaction mixture was heated to 80° C. and stirred overnight. When complete by LC/MS, the reaction was cooled to room temperature, quenched with HCl (0.5 N, 30 mL) and extracted with ethyl acetate (50 mL×3). The combined organic layers were dried over sodium sulfate, concentrated and dried under high vacuum. The resulting residue was purified by reverse phase chromatography using a mixture of acetonitrile and water to give compound 2 (50 mg, 20%).

1. temperatureWhen complete by LC/MS, the reaction was cooled to room temperature
2. customquenched with HCl (0.5 N, 30 mL)
3. extractionextracted with ethyl acetate (50 mL×3)
4. dry with materialThe combined organic layers were dried over sodium sulfate
5. concentrationconcentrated
6. customdried under high vacuum
7. customThe resulting residue was purified by reverse phase chromatography
8. additiona mixture of acetonitrile and water

ORD-Eintrag

ord-cecb897995984392a45da2e57c1dc05f

Quelldatensatz

uspto-grants-2014_07

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08772507B2