反応 #2286389

ord-e3e2337e3ae8460aa359d51a8c4c1c47

反応方程式

CN(C(=O)OC(C)(C)C)c1cnc(-c2cccnc2)s1
methyl-(2-pyridin-3-yl-thiazol-5-yl)-carbamic acid tert-butyl ester
O=C1CCC(=O)N1Br
N-bromosuccinimide
CN(C(=O)OC(C)(C)C)c1sc(-c2cccnc2)nc1Br
desired product
収率 64.3%
CN(C(=O)OC(C)(C)C)c1sc(-c2cccnc2)nc1Br
(4-bromo-2-pyridin-3-yl-thiazol-5-yl)-methyl-carbamic acid tert-butyl ester
収率 64.3%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    濃縮The reaction mixture was concentrated
  2. 2
    その他the crude product was purified by silica gel chromatography (0 to 100% ethyl acetate/hexanes)

実験手順

To a solution of methyl-(2-pyridin-3-yl-thiazol-5-yl)-carbamic acid tert-butyl ester (100 mg, 0.34 mmol) in acetonitrile (2 mL) was added N-bromosuccinimide (122 mg, 0.68 mmol) in one portion and the reaction mixture was stirred for 1 h. The reaction mixture was concentrated and the crude product was purified by silica gel chromatography (0 to 100% ethyl acetate/hexanes) to give the desired product as a white solid (81 mg, 64%): mp 88-91° C.; IR (KBr) 1715 cm−1; 1H NMR (300 MHz, CDCl3) δ 9.11 (s, 1H), 8.70 (d, J=4.2 Hz, 1H), 8.28-8.17 (m, 1H), 7.42 (dd, J=8.1, 4.8 Hz, 1H), 3.27 (s, 3H), 1.48 (s, 9H); ESIMS m/z 372 (M+2).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09357780B2uspto-grants-2016_06