Heterocyclic aspartyl protease inhibitors
A heteroaryl and solvate technology, applied in the field of heterocyclic aspartyl protease inhibitors, can solve problems such as not meeting medical requirements and not being able to prevent disease progression
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[0073] Compounds of formula I (wherein X, W and U are as defined above) include each of the following preferred structures:
[0074]
[0075] In compounds of formulas IA to IF, U is preferably a bond or -C(R 6 )(R 7 )-. In compounds of formula IG and IH, U is preferably -C(O)-.
[0076] It should be understood that since R 1 The definition of R 5 The definition of is the same, so when X is -N(R 5 )-, then W is a chemical bond and U is a chemical bond, -S(O)-, -S(O) 2 -, -C(O)-, -O-, -C(R 6 )(R 7 )-or-N(R 5 )-The compound of formula I is equivalent to U being a chemical bond and W being a chemical bond, -S(O)-, -S(O) 2 -, -C(O)-, -O-, -C(R 6 )(R 7 )-or-N(R 5 )- compound of formula I.
[0077] Compounds of the present invention are more preferably compounds of formula IB in which U is a chemical bond or U is -C(R 6 )(R 7 )- compound of formula IB.
[0078] Another preferred group of compounds of formula I are R 2 A compound of formula I which is H.
[0079] ...
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