Ethyl chloroformate → HCID 58382073, Verbindung

To a solution of 4-chloro-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridine (3.03 g, 9.81 mmol, Adesis) in THF (49 mL) at about −78° C. was added sec-BuLi (1.4 M in cyclohexane, 15.4 mL, 21.6 mmol) dropwise. The reaction was stirred at about −78° C. for about 1 h before ethyl chloroformate (2.36 mL, 24.5 mmol) was added rapidly. The reaction mixture was allowed to warm to ambient temperature and was stirred for about 40 min. The reaction was quenched with saturated aqueous NH4Cl (25 mL). EtOAc (50 mL) and water (50 mL) were added and the layers were separated. The aqueous layer was extracted with EtOAc (2×20 mL) and the combined organic layers were washed with brine (2×20 mL). The organics were dried over anhydrous Na2SO4, filtered, and concd to dryness under reduced pressure to give a yellow oil. The oil was purified by silica gel chromatography eluting with a gradient of 0-10% EtOAc in heptane to give ethyl 4-chloro-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridine-5-carboxylate (3.78 g, 98%) as a yellow oil: LC/MS (Table 1, Method b) Rt=3.98 min; MS m/z: 381 (M+H)+.

1. additionwas added rapidly
2. customThe reaction was quenched with saturated aqueous NH4Cl (25 mL)
3. additionEtOAc (50 mL) and water (50 mL) were added
4. customthe layers were separated
5. extractionThe aqueous layer was extracted with EtOAc (2×20 mL)
6. washthe combined organic layers were washed with brine (2×20 mL)
7. dry with materialThe organics were dried over anhydrous Na2SO4
8. filtrationfiltered
9. customconcd to dryness under reduced pressure to give a yellow oil
10. customThe oil was purified by silica gel chromatography
11. washeluting with a gradient of 0-10% EtOAc in heptane

ORD-Eintrag

ord-e6dc112ab6f34ab8afebf7da31af07d7

Quelldatensatz

uspto-grants-2013_04

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08426411B2