Hydrochloric Acid → 6-(2-fluorophenyl)-5H-pyrrolo[3,2-d]pyrimidine

温度

-20 °C

5-amino-4-methylpyrimidine (5 g, 45 mmol) was dissolved in 200 mL THF and cooled to −20° C. A solution of n-BuLi (112.5 mmol) was added over 10 minutes and the solution was kept at −20° C. for 30 min, then warmed to room temp and stirred for 3 h. It was then cooled to −40° C. and to it was added methyl-2-fluorobenzoate (1.75 mL, 13.7 mmol) and the solution stirred at −40° C. for 30 min and then warmed to room temp for 1 h. 50 mL of methanol was then added over 5 min, followed by 6N aq HCl. The solution was stirred for 18 h at room temp. It was then neutralized with NaHCO3 to pH 8 and then diluted with ethyl acetate and water. The organics were washed with water three times and then brine and dried over sodium sulfate and concentrated in vacuo. The crude material was purified by flash chromatography using 10% methanol/DCM. 1.5 g of product was isolated as a yellow solid (16%). 1H-NMR: (d6-DMSO, 400 MHz) δ 12.22 (s, 1H), 8.86 (s, 1H), 8.83 (s, 1H), 7.98(dt, 1H), 7.46 (m, 1H), 7.38 (m, 2H), 7.02(s, 1H) LC/MS: calculated for C12H8FN3: 213.2; found 214.10 (M+H)+.

1. temperaturewarmed to room temp
2. temperatureIt was then cooled to −40° C. and to it
3. stirringthe solution stirred at −40° C. for 30 min
4. temperaturewarmed to room temp for 1 h
5. stirringThe solution was stirred for 18 h at room temp
6. washThe organics were washed with water three times
7. dry with materialbrine and dried over sodium sulfate
8. concentrationconcentrated in vacuo
9. customThe crude material was purified by flash chromatography

ORDレコード

ord-c6cb8d8b46114681a4bdecd923c03fe7

出典データセット

uspto-grants-2014_08

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US08815858B2