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HRID1016968

反应详情

EQUATION

反应方程式

HRID 1016968 的结构方程式

REACTANTS

反应物

3
结构：C[C@H](NC(=O)Cc1ccccc1)C(=O)O
HCID7004640

未命名化合物

结构：COC(=O)[C@@H](N)CCCCNC(=O)OC(C)(C)C.Cl
HCID16218818

Methyl N~6~-(tert-butoxycarbonyl)-L-lysinate--hydrogen chloride (1/1)

C12H25ClN2O4

结构：CO.ClCCl.[NH4+].[OH-]
HCID21896990

未命名化合物

PRODUCTS

生成物

1
结构：COC(=O)[C@H](CCCCNC(=O)OC(C)(C)C)NC(=O)[C@H](C)NC(=O)Cc1ccccc1
HCID69734775

未命名化合物

PROCEDURE

实验过程

Following General Procedure A and using N-(phenylacetyl)-L-alanine (from Example B1 above) and Nε-(tert-butoxycarbonyl)-L-lysine methyl ester hydrochloride (Bachem), the title compound was prepared as a solid (mp=119-121° C.). The reaction was monitored by tlc (Rf=0.46 in 90:10:1 CH2Cl2/MeOH/NH4OH).