تفاعل #1994293

ord-ebc0e68d79b644a5b50996464b19963e

معادلة التفاعل

Nc1nc(-c2ccc(Cl)cc2F)nc(C(=O)O)c1Cl
6-amino-5-chloro-2-(4-chloro-2-fluorophenyl)-pyrimidine-4-carboxylic acid
Cl
HCl
CC(=O)Cl
acetyl chloride
CCCCCC.CCOC(C)=O
ethyl acetate hexane
CCOC(=O)c1nc(-c2ccc(Cl)cc2F)nc(N)c1Cl
title compound
المردود 63.5%
CCOC(=O)c1nc(-c2ccc(Cl)cc2F)nc(N)c1Cl
6-Amino-5-chloro-2-(4-chloro-2-fluorophenyl)pyrimidine-4-carboxylic acid ethyl ester
المردود 63.5%

المذيبات

ظروف التفاعل

درجة الحرارة
62°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةcooled in an ice bath
  2. 2
    تركيزThe reaction mixture was concentrated
  3. 3
    أخرىthe residue partitioned between ethyl acetate and water
  4. 4
    أخرىThe organic phase was dried
  5. 5
    تركيزconcentrated
  6. 6
    أخرىthe product was purified by column chromatography (dichloromethane/ethyl acetate gradient)

الإجراء التجريبي

A 1N solution of HCl in ethanol was generated by adding 0.565 mL of acetyl chloride dropwise to 12 mL of ethanol cooled in an ice bath. This solution was added to 200 mg of 6-amino-5-chloro-2-(4-chloro-2-fluorophenyl)-pyrimidine-4-carboxylic acid and the resulting solution was heated at 62° C. overnight. The reaction mixture was concentrated and the residue partitioned between ethyl acetate and water. The organic phase was dried and concentrated, and the product was purified by column chromatography (dichloromethane/ethyl acetate gradient). A second chromatography utilizing an amine-functionalized silica gel column (Biotage KP-NH) and an ethyl acetate/hexane gradient solvent system yielded the title compound (139 mg, 63.5% yield): mp 131-132° C.: 1H NMR (CDCl3): δ 7.97 (m, 1H), 7.2 (m, 2H), 5.63 (br s, 2H), 4.48 (q, 2H), 1.44 (t, 3H).

المصدر

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