反应 #8802
ord-bb34e2e93aa14e95ac75809f33844761
反应方程式
反应物
试剂
无
反应条件
详细条件
See reaction.notes.procedure_details.
后处理
- 1浓缩then concentrated in vacuo
- 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.