Long-acting low-addiction HNK derivative and preparation method therefor
AssigneeShenzhen Ruijian Biotechnology Co., Ltd
InventorsShu Peng Li, Qiang Zhou
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Abstract
The present application relates to a compound having the effects of being an antidepressant, anesthetizing, alleviating pain, improving cognitive functions, protecting lungs, preventing or treating amyotrophic lateral sclerosis or preventing or treating complex regional pain syndrome. Compared with existing known HNK compounds, the compound provided in the present application has a longer drug efficacy period. Moreover the compound provided in the present application basically does not produce addiction.
Claims15
A compound represented by Formula I, or a salt, stereoisomer or tautomer thereof:
- wherein,
- m is an integer from 0 to 3, and n is an integer from 0 to 4;
- R1 and R2 are each independently one or more selected from a group consisting of H, halogen, hydroxyl, amino, cyano, substituted or unsubstituted C1-C6 alkyl group, substituted or unsubstituted C2-C6 alkenyl group, substituted or unsubstituted C2-C6 alkynyl group, substituted or unsubstituted C3-C10 cycloalkyl group, substituted or unsubstituted C2-C10 heterocyclic group, substituted or unsubstituted C1-C6 alkoxy group, substituted or unsubstituted mono- and di-C1-C6 alkylamino group, substituted or unsubstituted aryl group, and substituted or unsubstituted heteroaryl group;
- R3 is halogen;
- R4 is selected from a group consisting of H, substituted or unsubstituted C1-C6 alkyl group, substituted or unsubstituted C1-C8 acyl group, substituted or unsubstituted arylacyl group, and substituted or unsubstituted heteroarylacyl group;
- R5 is selected from a group consisting of substituted or unsubstituted C3-C10 cycloalkylene group, substituted or unsubstituted C2-C10 heterocyclylene group, substituted or unsubstituted arylene group, and substituted or unsubstituted heteroarylene group;
- R6 and R7 are independently selected from a group consisting of H, substituted or unsubstituted C1-C6 alkyl group, substituted or unsubstituted C2-C6 alkenyl group, substituted or unsubstituted C2-C6 alkynyl group, substituted or unsubstituted C3-C10 cycloalkyl group, substituted or unsubstituted C2-C10 heterocyclic group, substituted or unsubstituted aryl group, substituted or unsubstituted heteroaryl group, substituted or unsubstituted C1-C8 acyl group, substituted or unsubstituted arylacyl group, and substituted or unsubstituted heteroaryl acyl,
- or R6 and R7, together with N atom to which R6 and R7 are connected, form a substituted or unsubstituted 3 to 10-membered monocyclic or bicyclic structure,
- wherein a group is substituted means that the group is substituted by a substituent selected from OH;
- NH2;
- C1-C10 alkyl, alkenyl or alkynyl group;
- C1-C10 alkylamine group;
- sulfhydryl group;
- C1-C10 alkylsulfhydryl group;
- C1-C20 alkoxy group;
- C1-C10 carbonyl group;
- C3-C10 cycloalkyl group;
- 3 to 10-membered heterocyclic group with one or more heteroatoms selected from N, S, O and P;
- C6-C20 aryl group;
- C2-C20 heteroaryl group;
- nitrocyano;
- and halogen.
A compound, or a salt, stereoisomer or tautomer thereof, wherein the compound is shown below:
- wherein R8 is H or a protecting group.
Dependencies are inferred from the claim text.