反应 #69628
ord-16c12e29c27c4e31ace7baeccc73080c
反应方程式
hydrochloride monohydrate
compound IV
hydrochloride monohydrate
ethyl-N-(6-amino-2,3-dichlorobenzyl)glycine
compound I
ethyl-N-(6-amino-2,3-dichlorobenzyl)glycine
cyanogen bromide
anagrelide
cyanogen bromide
→
compound II
iminoquinazoline
反应物
试剂
无
溶剂
反应条件
详细条件
See reaction.notes.procedure_details.
实验过程
Commercially, as discussed in U.S. Pat. No. 5,801,245, and as shown in FIG. 1, anagrelide has been prepared as the hydrochloride monohydrate (compound IV) from the intermediate, ethyl-N-(6-amino-2,3-dichlorobenzyl)glycine (compound I) either by reaction with cyanogen bromide in hot alcoholic solution, or, preferentially, by reaction with cyanogen bromide in an aprotic solvent such as toluene to give the iminoquinazoline intermediate (compound II), which is isolated and then reacted with a base in a hot solution of alcohol to form anagrelide base (compound III).