تفاعل #5031

ord-d6f8a145407c4859b6e938637fa82e5b

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe pH of reaction mixture
  2. 2
    استخلاصthe mixture extracted with 250 ml ethyl acetate
  3. 3
    استخلاصThe aqueous layer was further extracted with 2×50 ml of 1:1 THF
  4. 4
    تجفيفdried over Na2SO4
  5. 5
    أخرىevaporated to a solid, which
  6. 6
    أخرىwas recrystallized from ethyl acetate
  7. 7
    أخرىto yield
  8. 8
    أخرىpurified title product, 17.8 g (50.7%)

الإجراء التجريبي

Under nitrogen, 14 g (0.29 mmol) of 50% NaH in oil was washed with 2×40 ml of hexane and then suspended in 90 ml of anhydrous tetrahydrofuran (THF). To this slurry at 0° C. was added dropwise a solution of ethyl 2-(2-amino-4-thiazolyl)acetate (27 g, 0.145 mmol) in 290 ml of anhydrous THF, followed by ethyl formate (21.5 g, 0.29 mmol), and the mixture stirred at room temperature for 18 hours. The pH of reaction mixture was adjusted to 7 by the addition of 50% aqueous acetic acid and the mixture extracted with 250 ml ethyl acetate. The aqueous layer was further extracted with 2×50 ml of 1:1 THF:ethyl acetate. The extracts were combined, dried over Na2SO4 and evaporated to a solid, which was recrystallized from ethyl acetate to yield purified title product, 17.8 g (50.7%); m.p. 179°-180° C.; 1H-nmr (CDCl3 -d6 -DMSO) 1.33 (t, 3H), 4.16 (q, 2H), 7.50 (s, 1H), 8.00 (s, 1H), 8.53 (s, 1H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05242913uspto-grants-1993_09