تفاعل #1994291

ord-57e05fd18ab3467c803cd5060c5309ba

معادلة التفاعل

COC(=O)c1nc(Cl)nc(N)c1Cl
6-Amino-2,5-dichloropyrimidine-4-carboxylic acid methyl ester
[Cs+].[F-]
cesium fluoride
OB(O)c1ccc(Cl)cc1F
4-chloro-2-fluorophenylboronic acid
COC(=O)c1nc(-c2ccc(Cl)cc2F)nc(N)c1Cl
title compound
المردود 40.8%
COC(=O)c1nc(-c2ccc(Cl)cc2F)nc(N)c1Cl
6-Amino-5-chloro-2-(4-chloro-2-fluorophenyl)pyrimidine-4-carboxylic acid methyl ester
المردود 40.8%

ظروف التفاعل

درجة الحرارة
100°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe cooled reaction mixture
  2. 2
    غسيلwashed with water
  3. 3
    أخرىdried
  4. 4
    تركيزconcentrated
  5. 5
    أخرىThe product was purified by column chromatography (methylene chloride/ethyl acetate gradient)
  6. 6
    أخرىthen purified again by column chromatography (ethyl acetate/hexane gradient)

الإجراء التجريبي

6-Amino-2,5-dichloropyrimidine-4-carboxylic acid methyl ester (1.11 g, 5 mmol, see WO 2007/082076 A1 for preparation), 4-chloro-2-fluorophenylboronic acid (1.13 g, 6.5 mmol), bis(triphenylphosphine)-palladium(II) dichloride (350 mg, 0.5 mmol), and cesium fluoride (1.52 g, 10 mmol) were combined in 10 mL of 1,2-dimethoxyethane (DME) and 10 mL of water. The reaction mixture was heated in a CEM microwave at 100° C. for 15 minutes. The cooled reaction mixture was diluted with ethyl acetate, washed with water, dried and concentrated. The product was purified by column chromatography (methylene chloride/ethyl acetate gradient) then purified again by column chromatography (ethyl acetate/hexane gradient) to yield the title compound (574 mg, 40.8% yield): mp 194-196° C.; 1H NMR (CDCl3): δ 7.96 (m, 1H), 7.2 (m, 2H), 5.64 (br s, 2H), 4.01 (s, 3H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08598085B2uspto-grants-2013_12