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HRID400825

反应详情

EQUATION

反应方程式

HRID 400825 的结构方程式

REACTANTS

反应物

3
结构：CC(C)(C)c1nc(N2CCOCC2)c2nnn(Cc3ccccc3Cl)c2n1
HCID1433953

未命名化合物

结构：Cl.O[C@@H]1CCCNC1
HCID2759333

(3R)-3-Hydroxypiperidine hydrochloride

C5H12ClNO

结构：CC(C)(C)c1nc(Cl)c2nnn(Cc3ccccc3Cl)c2n1
HCID86683284

5-tert-butyl-7-chloro-3-(2-chlorobenzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine

C15H15Cl2N5

PRODUCTS

生成物

1
结构：CC(C)(C)c1nc(N2CCC[C@@H](O)C2)c2nnn(Cc3ccccc3Cl)c2n1
HCID71557723

未命名化合物

PROCEDURE

实验过程

In analogy to the procedure described for the synthesis of 5-tert-butyl-3-(2-chloro-benzyl)-7-morpholin-4-yl-3H-[1,2,3]triazolo[4,5-d]pyrimidine (example 1, step c), the title compound was prepared from 5-tert-butyl-7-chloro-3-(2-chlorobenzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine and (R)-piperidin-3-ol hydrochloride and isolated as colorless gum (8.3 mg, 44%). MS (m/e): 401.4 (MH+).