HRID2209047

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID2795301

4-Methyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydro-2H-1,4-benzoxazine

C15H22BNO3

结构：C[C@@H](Oc1nc(Cl)cc2ncn(C)c12)[C@H]1CNC(=O)C1

HCID117843294

未命名化合物

PRODUCTS

生成物

结构：C[C@@H](Oc1nc(-c2ccc3c(c2)OCCN3C)cc2ncn(C)c12)[C@H]1CNC(=O)C1

HCID117843987

未命名化合物

PROCEDURE

实验过程

Following General Procedure B, beginning with (R)-4-((R)-1-(6-chloro-3-methyl-3H-imidazo[4,5-c]pyridin-4-yloxy)ethyl)pyrrolidin-2-one 2.06 (22.1 mg, 0.075 mmol) and 4-methyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydro-2H-benzo[b][1,4]oxazine (25 mg, 0.091 mmol) (R)-4-((R)-1-(3-methyl-6-(4-methyl-3,4-dihydro-2H-benzo[b][1,4]oxazin-7-yl)-3H-imidazo[4,5-c]pyridin-4-yloxy)ethyl)pyrrolidin-2-one 3B.06 was synthesized.

WORKUP

后处理

customwas synthesized