反应 #1914880

ord-121d42bbce42469fa0695ddb32a8e832

反应方程式

Br.Nc1nc(N)c2nc(CBr)ccc2n1
2,4-diamino-6-bromomethylpyrido[3,2-d]pyrimidine hydrobromide
c1ccc2c(c1)[nH]c1ccccc12
carbazole
Nc1nc(N)c2nc(CN(c3ccccc3)c3ccccc3)cnc2n1
N-[(2,4-diaminopteridin-6-yl)methyl]-N,N-diphenylamine
[H-].[Na+]
NaH
Nc1nc(N)c2nc(Cn3c4ccccc4c4ccccc43)ccc2n1
N-[(2,4-Diaminopyrido[3,2-d]pyrimidin-6-yl)methyl]carbazole

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The product can be purified by chromatography

实验过程

N-[(2,4-Diaminopyrido[3,2-d]pyrimidin-6-yl)methyl]carbazole (Formula I: Ar=2,4-diaminopyrido[2,3-d]pyrimidin-6-yl; W=CH2; X=N; Z=chemical bond; m=n=0) is prepared similarly to N-[(2,4-diaminopteridin-6-yl)methyl]-N,N-diphenylamine as disclosed above by using carbazole (129 mg, 0.77 mmol), NaH (50 mg, 2.1 mmol), and 2,4-diamino-6-bromomethylpyrido[3,2-d]pyrimidine hydrobromide (100 mg, 0.3 mmol). The product can be purified by chromatography.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07056911B1uspto-grants-2006_06