Boron trifluoride etherate → 1-(5-Bromopyridin-2-yl)cyclopropan-1-amine

温度

-78 °C

5-bromopicolinonitrile (D9) (43.6 g, 0.238 mol) was suspended in diethyl ether (1.3 L) and the resulting mixture was cooled to −78° C. Titanium (IV) isopropoxide (74.4 g, 0.262 mol) was added dropwise and the reaction mixture was stirred for 5 min. Ethylmagnesium bromide 1M in diethyl ether (525 ml, 0.525 mol) was added dropwise and the resulting reaction mixture was stirred for 30 mins at −78° C. The reaction mixture was allowed to warm to room temperature for 1 hour then boron trifluoride etherate (107 ml) was added dropwise. After stirred at room temperature for 2 hours, the reaction was quenched with 1M HCl (1.5 L). The aqueous layer was washed with diethyl ether (1 L) and then basified (pH=9) with 2N NaOH (1.25 L). The resulting mixture was extracted with ethyl acetate. The organic layer was dried over Na2SO4 and evaporated in vacuo. The residue was purified by column chromatography eluting with a mixture petroleum ether/ethyl acetate 1:1. Collected fractions after solvent evaporation afforded the title compound (D10) (15.7 g) as a grey solid.

1. customthe resulting reaction mixture
2. stirringwas stirred for 30 mins at −78° C
3. temperatureto warm to room temperature for 1 hour
4. stirringAfter stirred at room temperature for 2 hours
5. customthe reaction was quenched with 1M HCl (1.5 L)
6. washThe aqueous layer was washed with diethyl ether (1 L)
7. extractionThe resulting mixture was extracted with ethyl acetate
8. dry with materialThe organic layer was dried over Na2SO4
9. customevaporated in vacuo
10. customThe residue was purified by column chromatography
11. washeluting with a mixture petroleum ether/ethyl acetate 1:1
12. customCollected fractions after solvent evaporation

ORDレコード

ord-18dce512ce704e37946040297c861361

出典データセット

uspto-grants-2014_09

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US08828987B2