반응 #1144436

ord-aaafb6d740874c32a1bd59e0e0b2beee

반응 방정식

CC(=O)O
acetic acid
CC(C)[N-]C(C)C.[Li+]
lithium diisopropylamide
CCCCn1cc(CC)c(=O)[nH]c1=O
1-butyl-5-ethyluracil
C1CCOC1
tetrahydrofuran
C1CCOC1
tetrahydrofuran
c1ccc(SSc2ccccc2)cc1
diphenyl disulfide
C1CCOC1
tetrahydrofuran
CCCCn1c(-c2ccccc2)c(CC)c(=O)[nH]c1=S
1-butyl-5-ethyl-6-phenylthiouracil
수율 7.0%

반응 조건

온도
-25°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The mixture was cooled to −70° C. again
  2. 2
    workup.STIRRINGstirred for 20 minutes
  3. 3
    기타brought to room temperature
  4. 4
    세척washed with saturated aqueous solution of sodium chloride
  5. 5
    농축concentrated under reduced pressure
  6. 6
    세척eluted with 10% ethyl acetate/hexane
  7. 7
    기타crystallized from hexane

실험 절차

Then, a solution of 4.4 mmol of lithium diisopropylamide in 2.8 ml of tetrahydrofuran was added dropwise to a solution of 392 mg (2.0 mmol) 1-butyl-5-ethyluracil in 9 ml of tetrahydrofuran under a nitrogen atmosphere at −70° C. and stirred for 70 minutes at −70° C. and further 5 minutes at −25° C. The mixture was cooled to −70° C. again, added with a solution of 567 mg (2.6 mmol) diphenyl disulfide in 3 ml of tetrahydrofuran, stirred for 20 minutes, added with 1 ml of acetic acid, brought to room temperature, washed with saturated aqueous solution of sodium chloride and concentrated under reduced pressure. The residue was adsorbed on a silica gel, eluted with 10% ethyl acetate/hexane and crystallized from hexane to obtain 40 mg of 1-butyl-5-ethyl-6-phenylthiouracil (Yield: 7%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: USRE037979E1uspto-grants-2003_02