反应 #1914887

ord-2e692b5d60724436acb8f30162fc65f5

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The final product and its intermediates can b purified by chromatography

实验过程

N-[(2,4-Diaminothieno[2,3-d]pyrimidin-5-yl)methyl]-9,10-dihydroacridine (Formula I: Ar=2,4-diaminothieno[2,3-d]pyrimidi-5-yl; W=CH2; X=N; Z=CH2; m=n=0) is prepared similarly to N-[(2,4-diaminothieno[2,3-d]pyrimidin-5-yl)methyl]-N,N-diphenylamine as disclosed in Example 11 above by using 2,4-diamino-5-methylthieno[2,3-d]pyrimidine (1.3 g, 7.4 mmol) in Step 1 and 9,10-dihydroacridine (134 mg, 0.8 mmol) in Step 3. The final product and its intermediates can b purified by chromatography.

来源

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