反应 #8802

ord-bb34e2e93aa14e95ac75809f33844761

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    浓缩then concentrated in vacuo
  2. 2
    其他the residue dried

实验过程

Ester 40 (828 mg, 2.25 mmol), prepared as described above, was treated with a 6:4 mixture of methylene chloride:trifluoroacetic acid (8 ml). The solution was stirred for 20 min then concentrated in vacuo and the residue dried to give methyl 2-(3-amino-4-thienyl)-4,5-dihydroxy-pyrimidine-6-carboxylate trifluoroacetate (860 mg, 99%) as a solid. 1H NMR (DMSO-d6): δ 8.32 (1H, s), 6.75 (1H, s), 3.87 (3H, s). MS m/z (MH)+ 268.0.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07091209B2uspto-grants-2006_08