Dimethylformamide → HCID 57546090, 화합물

To a solution of 7-bromo-5-methoxy-1H-indazole (1.32 g, 5.81 mmol) in tetrahydrofuran (27 mL) at 0° C. was added sodium hydride (0.465 g, 11.62 mmol). The ice bath was removed and stirring continued for 20 min. The solution was cooled to −78° C. and treated with tert-butyllithium (1.7 M in pentane, 6.84 mL, 11.63 mmol) dropwise. The reaction was stirred at −78° C. for 10 min, allowed to warm gradually in the dewar to −50° C., recooled to −78° C., and then treated with dimethylformamide (1.8 mL, 23.25 mmol). After 15 min, the ice bath was removed and stirring continued for 1 h. The reaction was poured onto ice/1 M hydrochloric acid (20 mL). The mixture was extracted with ethyl acetate (2×). The organics were washed with water, then brine, dried over magnesium sulfate, and concentrated to give 1.1 g of 5-methoxy-1H-indazole-7-carbaldehyde (100%) as a tan solid. 1H-NMR (CDCl3, 300 MHz) δ 10.08 (s, 1H), 8.04 (s, 1H), 7.52 (s, 1H), 7.44 (m, 1H), 3.90 (s, 3H); Mass spec.: 177.09 (MH)+.

1. customThe ice bath was removed
2. stirringThe reaction was stirred at −78° C. for 10 min
3. temperatureto warm gradually in the dewar to −50° C.
4. customrecooled to −78° C.
5. waitAfter 15 min
6. customthe ice bath was removed
7. stirringstirring
8. waitcontinued for 1 h
9. additionThe reaction was poured onto ice/1 M hydrochloric acid (20 mL)
10. extractionThe mixture was extracted with ethyl acetate (2×)
11. washThe organics were washed with water
12. dry with materialbrine, dried over magnesium sulfate
13. concentrationconcentrated

ORD 기록

ord-bfb09c6de9d14e13a79625163b9f4163

출처 데이터셋

uspto-grants-2011_09

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US08026257B2