تفاعل #62723

ord-991fd2a5e38d4a84a08c0fd825d64fa8

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةheated on a steam bath for 4 hr
  2. 2
    درجة الحرارةThe reaction mixture was cooled to 50°
  3. 3
    workup.ADDITIONpoured onto ice (100 g)
  4. 4
    workup.STIRRINGwith stirring
  5. 5
    أخرىgiving a suspension which
  6. 6
    استخلاصwas then extracted with methylene chloride (3×100 mL)
  7. 7
    غسيلThe combined extracts were washed with 0.1N sodium hydroxide (2×100 mL), water (100 mL)
  8. 8
    تجفيفdried over anhydrous magnesium sulfate
  9. 9
    أخرىEvaporation of solent in vacuo

الإجراء التجريبي

A mixture of 2,4-diamino-5-(3-hydroxy-4,5-dimethoxybenzyl)pyrimidine (2.76 g, 0.01 mole) and crotonic acid (0.87 g, 0.01 mole) in polyphosphoric acid (27 g) was stirred and heated on a steam bath for 4 hr. The reaction mixture was cooled to 50° and poured onto ice (100 g) with stirring. The resulting solution was basified to pH 8.0 with concentrated ammonium hydroxide, giving a suspension which was then extracted with methylene chloride (3×100 mL). The combined extracts were washed with 0.1N sodium hydroxide (2×100 mL), water (100 mL) and then dried over anhydrous magnesium sulfate. Evaporation of solent in vacuo gave the title compound (1.0 g, 29%). This was recrystallised from 95% ethanol to give 2,4-diamino-5-(3,4-dihydro-7,8-dimethoxy-2-methyl-4-oxo-2H-1-benzopyran-5-ylmethyl)pyrimidine as the hemihydrate, mp 128°-132°. Anal. Calcd for C17H20N4O4.1/2H2O: C, 57.78; H, 5.99; N, 15.85. Found: C, 57.79; H, 6.02; N, 15.86.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04761475uspto-grants-1988_08