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HRID400958

反应详情

EQUATION

反应方程式

HRID 400958 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：CC(=O)N[C@H]1CCNC1
HCID7021471

(3S)-(-)-3-Acetamidopyrrolidine

C6H12N2O

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(=O)N[C@H]1CCN(c2nc(C(C)(C)C)nc3c2nnn3Cc2ccccc2Cl)C1
HCID86683369

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-chlorobenzyl)-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 (S)—N-(pyrrolidin-3-yl)acetamide. MS (m/e): 428.3 (MH+).