反应 #1885067

ord-70702f0944614685891d1bdac5c841ca

反应方程式

C#Cc1cccc(Nc2ncnc3cc(OC(C)=O)c(OC(C)=O)cc23)c1.Cl
14
C#Cc1cccc(Nc2ncnc3cc(OC(C)=O)c(OC(C)=O)cc23)c1.Cl
N-(3-ethynylphenyl)-6,7-diacetoxy-4-quinazolinamine hydrochloride
N
ammonia
C#Cc1cccc(Nc2ncnc3cc(O)c(O)cc23)c1.Cl
15
收率 93.0%
C#Cc1cccc(Nc2ncnc3cc(O)c(O)cc23)c1.Cl
N-(3-ethynylphenyl)-6,7-dihydroxy-4-quinazolinamine hydrochloride
收率 93.0%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    过滤The reaction mass was filtered
  2. 2
    洗涤the solid was washed with water

实验过程

To the hydrochloride salt, 14 (4.2 g, 11.62 mmol) in methanol (30 ml) was added 25% aqueous ammonia (4.73 ml) and the solution was stirred for 4 h. The reaction mass was filtered and the solid was washed with water to give the N-(3-ethynylphenyl)-6,7-dihydroxy-4-quinazolinamine hydrochloride, 15 (3.0 g, 93%) as a brownish yellow solid. 1H NMR (400 MHz, DMSO-d6): 4.2 (s, 1H), 7.10 (s, 1H), 7.17-7.19 (m, 2H), 7.34-7.39 (t, 1H), 7.79 (s, 1H), 7.87-7.89 (d, 1H), 8.05 (s, 1H), 8.45 (s, 1H), 9.4-9.6 (bs. s, 1H). MS (ESI): 278.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08343950B2uspto-grants-2013_01