تفاعل #40609

ord-97b2d45e987f4f5581a86c3d7fc3bcd7

معادلة التفاعل

CCOC(=O)CCN(c1ccc2c(c1)CCC2)c1nc(SC)ncc1C(=O)OCC
4-[(2-ethoxycarbonyl-ethyl)-indan-5-yl-amino]-2-methylsulfanyl-pyrimidine-5-carboxylic acid ethyl ester
CC(C)(C)[O-].[Na+]
sodium t-butoxide
N#N
N2
Cl
HCl
[Na]
sodium
CCOC(=O)C1CN(c2ccc3c(c2)CCC3)c2nc(SC)ncc2C1=O
8-Indan-5-yl-2-methylsulfanyl-5-oxo-5,6,7,8-tetrahydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid ethyl ester

المذيبات

ظروف التفاعل

درجة الحرارة
90°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe solution was cooled
  2. 2
    workup.ADDITIONpoured
  3. 3
    أخرىinto crushed ice
  4. 4
    استخلاصThe precipitates were extracted into EtOAc twice
  5. 5
    أخرىThe solvent was evaporated under vacuum
  6. 6
    أخرىthe product (bright yellow solid, 4 g, 62%) was recrystallized from isopropanol

الإجراء التجريبي

To sodium (25 wt % dispersion in paraffin wax, 1.6 g, 16.9 mmol) was added t-butanol (30 mL) under stirring and N2. After 10 minutes, a solution of 4-[(2-ethoxycarbonyl-ethyl)-indan-5-yl-amino]-2-methylsulfanyl-pyrimidine-5-carboxylic acid ethyl ester (6.6 g, 15.4 mmol) in 40 mL of toluene was added to the sodium t-butoxide solution. The mixture was then heated at 90° C. for 30 minutes. The solution was cooled and poured into crushed ice. The solution was adjusted to pH 7 using HCl solution. The precipitates were extracted into EtOAc twice. The solvent was evaporated under vacuum and the product (bright yellow solid, 4 g, 62%) was recrystallized from isopropanol. 1H NMR (300 MHz, CDCl3) indicated that the presence of both enol and keto forms in a 4:1 ratio.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07728003B2uspto-grants-2010_06