تفاعل #2075733

ord-5b8cb3e1963e480f9284bc31dc2ba1d7

معادلة التفاعل

COC(=O)c1nc(-c2ccc(Cl)c(OC)c2F)nc(N)c1SC
6-amino-2-(4-chloro-2-fluoro-3-methoxyphenyl)-5-methylsulfanyl-pyrimidine-4-carboxylic acid methyl ester
[Na+].[OH-]
sodium hydroxide
Cl
HCl
COc1c(Cl)ccc(-c2nc(N)c(SC)c(C(=O)O)n2)c1F
title compound
المردود 70.6%
COc1c(Cl)ccc(-c2nc(N)c(SC)c(C(=O)O)n2)c1F
6-Amino-2-(4-chloro-2-fluoro-3-methoxyphenyl)-5-methylsulfanyl-pyrimidine-4-carboxylic acid
المردود 70.6%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزThe resulting solution was concentrated
  2. 2
    أخرىpartitioned between ethyl acetate and water
  3. 3
    أخرىThe organic phase was dried
  4. 4
    تركيزconcentrated

الإجراء التجريبي

6-amino-2-(4-chloro-2-fluoro-3-methoxyphenyl)-5-methylsulfanyl-pyrimidine-4-carboxylic acid methyl ester (100 mg, 0.28 mmol) was dissolved in 2 mL methanol and 0.5 mL of 2N sodium hydroxide (1 mmol) was added. The reaction mixture was stirred at room temperature for 4 h and then acidified with a slight excess of 2N HCl. The resulting solution was concentrated and partitioned between ethyl acetate and water. The organic phase was dried and concentrated to yield the title compound (68 mg, 70% yield): mp 153° C. (dec.): 1H NMR (CDCl3): δ 7.63 (m, 1H), 7.2 (m, 1H), 6.4 (br s, 2H), 3.98 (s, 3H), 2.42 (s, 3H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07642220B2uspto-grants-2010_01