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HRID881488

反应详情

EQUATION

反应方程式

HRID 881488 的结构方程式

REACTANTS

反应物

4
结构：Cl
HCID313

Hydrochloric Acid

ClH

结构：O=C(O)C(F)(F)F
HCID6422

未命名化合物

结构：C[C@H](NC(=O)OC(C)(C)C)C(=O)O
HCID85082

L-Alanine, N-[(1,1-dimethylethoxy)carbonyl]-

C8H15NO4

结构：Cc1c(CN2CCNCC2)sc2c(N3CCOCC3)nc(-c3cnc(N)nc3)nc12
HCID56648673

未命名化合物

PRODUCTS

生成物

1
结构：Cc1c(CN2CCN(C(=O)[C@H](C)N)CC2)sc2c(N3CCOCC3)nc(-c3cnc(N)nc3)nc12
HCID56648677

未命名化合物

收率 61%

PROCEDURE

实验过程

Crude HCl salt of 5-(7-methyl-4-morpholino-6-(piperazin-1-ylmethyl)thieno[3,2-d]pyrimidin-2-yl)pyrimidin-2-amine (74 mg) was reacted with 60 mg Boc-L-Alanine via General Procedure B, treated with TFA and purified via reverse phase HPLC to yield 52.7 mg of 354 after reverse phase HPLC purification. MS (Q1) 498.3 (M)+

WORKUP

后处理

  1. custompurified via reverse phase HPLC