Iodine → tert-Butyl (6-chloro-4-iodopyridin-3-yl)carbamate

温度

-78 °C

To a solution of TMEDA (1.45 g, 12.5 mmol) in dry Et2O (30 mL) was added dropwise n-BuLi (5.0 mL, 12.5 mmol) at −78° C. The mixture was stirred for 0.5 h at −78° C. A solution of (6-chloro-pyridin-3-yl)-carbamic acid tert-butyl ester (1.14 g, 5.0 mmol) in dry Et2O (10 mL) was added dropwise to the reaction mixture at −78° C. and the resultant mixture was continued to stir for 1 h at −78° C. A solution of I2 (1.52 g, 6.0 mmol) in dry Et2O (10 mL) was added dropwised at −78° C. The mixture was continued to stir for 1 h at this temperature. The reaction was quenched with saturated aqueous NH4Cl. The organic layer was separated and the aqueous phase was extracted with ethyl acetate (50 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and evaporated under reduced pressure to give a residue, which was purified by column (petroleum ether/ethyl acetate=10/1) to obtain (6-chloro-4-iodo-pyridin-3-yl)-carbamic acid tert-butyl ester (1.75 g, 30%). 1H NMR (400 MHz, CDCl3) δ 8.95 (br s, 1H), 7.73 (s, 1H), 6.64 (br s, 1H), 1.54 (s, 1H).

1. stirringto stir for 1 h at −78° C
2. customdropwised at −78° C
3. stirringto stir for 1 h at this temperature
4. customThe reaction was quenched with saturated aqueous NH4Cl
5. customThe organic layer was separated
6. extractionthe aqueous phase was extracted with ethyl acetate (50 mL×3)
7. dry with materialThe combined organic layers were dried over anhydrous Na2SO4
8. customevaporated under reduced pressure
9. customto give a residue, which
10. customwas purified by column (petroleum ether/ethyl acetate=10/1)

ORDレコード

ord-f3e592f1aaf5493b94e434d610cd2d92

出典データセット

uspto-grants-2015_08

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US09102672B2