반응 #2075725

ord-9902130fed2c4a46bf5f65f8b434dfa3

반응 방정식

COC(=O)c1nc(Cl)nc(N)c1OC
6-Amino-2-chloro-5-methoxypyrimidine-4-carboxylic acid methyl ester
[Cs+].[F-]
cesium fluoride
COc1c(Cl)ccc(B(O)O)c1F
4-chloro-2-fluoro-3-methoxyphenylboronic acid
COC(=O)c1nc(-c2ccc(Cl)c(OC)c2F)nc(N)c1OC
title compound
수율 52.7%
COC(=O)c1nc(-c2ccc(Cl)c(OC)c2F)nc(N)c1OC
6-amino-2-(4-chloro-2-fluoro-3-methoxyphenyl)-5-methoxypyrimidine-4-carboxylic acid methyl ester
수율 52.7%

반응 조건

온도
100°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The cooled reaction mixture
  2. 2
    세척washed with water
  3. 3
    세척washed with brine
  4. 4
    기타dried
  5. 5
    농축concentrated
  6. 6
    기타The product was purified by flash chromatography on silica gel (hexane/ethyl acetate gradient)

실험 절차

6-Amino-2-chloro-5-methoxypyrimidine-4-carboxylic acid methyl ester (0.2 g, 0.9 mmol), 4-chloro-2-fluoro-3-methoxyphenylboronic acid (0.29 g, 1.4 mmol), bis(triphenylphosphine)palladium(II) dichloride (65 mg, 0.1 mmol), and cesium fluoride (0.28 g, 1.9 mmol) were combined in 1 mL of 1,2-dimethoxyethane and 1 mL of water. The reaction mixture was heated in a CEM microwave at 100° C. for 15 min (other temperature/time pairs used in the subsequent examples were 110° C. for 15 min and 150° C. for 5 min). The cooled reaction mixture was diluted with ethyl acetate, washed with water, washed with brine, dried and concentrated. The product was purified by flash chromatography on silica gel (hexane/ethyl acetate gradient) to yield the title compound (162 mg, 51.1% yield): mp 155-158° C.; 1H NMR (CDCl3): δ 7.58 (dd, 1H), 7.20 (dd, 1H), 5.56 (br s, 2H) 4.00 (s, 3H), 3.99 (d, 3H), 3.94 (s, 3H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07642220B2uspto-grants-2010_01