Long-acting low-addiction HNK derivative and preparation method therefor
The present application relates to a compound having the functions of being an antidepressant, improving anxiety and post-traumatic stress syndrome, anesthetizing, easing pain, improving cognitive function, protecting the lungs, preventing or treating amyotrophic lateral sclerosis or preventing or treating complex regional pain syndrome. Compared with existing known HNK compounds, the compound of the present invention has a longer drug efficacy period, and the compound of the present invention essentially does not lead to addiction.
1 . A compound represented by Formula III, or a salt, stereoisomer or tautomer thereof:
wherein,
m is an integer from 0 to 3, n is an integer from 0 to 4, and p is an integer from 0 to 3;
R 1 and R 2 are each independently one or more selected from a group consisting of H, halogen, hydroxyl, amino, cyano, substituted or unsubstituted C 1 -C 6 alkyl group, substituted or unsubstituted C 2 -C 6 alkenyl group, substituted or unsubstituted C 2 -C 6 alkynyl group, substituted or unsubstituted C 3 -C 10 cycloalkyl group, substituted or unsubstituted C 2 -C 10 heterocyclic group, substituted or unsubstituted C 1 -C 6 alkoxy group, substituted or unsubstituted mono- and di-C 1 -C 6 alkylamino group, substituted or unsubstituted aryl group, and substituted or unsubstituted heteroaryl group;
R 3 is halogen;
R 4 is selected from a group consisting of H, substituted or unsubstituted C 1 -C 6 alkyl group, substituted or unsubstituted C 1 -C 8 acyl group, substituted or unsubstituted arylacyl group, and substituted or unsubstituted heteroarylacyl group;
R 6 is selected from a group consisting of H, substituted or unsubstituted C 1 -C 6 alkyl group, substituted or unsubstituted C 2 -C 6 alkenyl group, substituted or unsubstituted C 2 -C 6 alkynyl group, substituted or unsubstituted C 3 -C 10 cycloalkyl group, substituted or unsubstituted C 2 -C 10 heterocyclic group, substituted or unsubstituted aryl group, substituted or unsubstituted heteroaryl group, substituted or unsubstituted C 1 -C 8 acyl group, substituted or unsubstituted arylacyl group, and substituted or unsubstituted heteroaryl acyl,
wherein a group is substituted means that the group is substituted by a substituent selected from OH; NH 2 ; C 1 -C 10 alkyl, alkenyl or alkynyl group; C 1 -C 10 alkylamine group; sulfhydryl group; C 1 -C 10 alkylsulfhydryl group; C 1 -C 20 alkoxy group; C 1 -C 10 carbonyl group; C 3 -C 10 cycloalkyl group; 3 to 10-membered heterocyclic group with one or more heteroatoms selected from N, S, O and P; C 6 -C 20 aryl group; C 2 -C 20 heteroaryl group; nitrocyano; and halogen.
2 . The compound according to claim 1 , represented by Formula IV:
3 . The compound according to claim 1 , wherein the compound is shown below:
4 . The compound according to claim 1 , wherein the compound is shown below:
5 . A compound, or a salt, stereoisomer or tautomer thereof, wherein the compound is shown below:
wherein Ry is H or a protecting group.
6 . The compound according to claim 5 , wherein the compound is shown below:
7 . The compound according to claim 5 , wherein the compound is shown below:
8 . A pharmaceutical composition, comprising the compound, or the salt, stereoisomer or tautomer thereof according to claim 1 , and optionally a pharmaceutically acceptable carrier.
9 . A pharmaceutical composition, comprising the compound, or the salt, stereoisomer or tautomer thereof according to claim 5 , and optionally a pharmaceutically acceptable carrier.
10 . A preparation method of a compound (I 6 ), wherein the preparation method comprises steps of:
esterifying a compound (G) to produce product (H 6 ); and
deprotecting the product (H 6 ) to produce the compound (I 6 ),
11 . A method for anesthesia, alleviating pain, improving cognitive function, lung protection, anti-depression, mitigating anxiety and post-traumatic stress syndrome, or preventing or treating amyotrophic lateral sclerosis or complex regional pain syndrome of a subject, comprising administrating a therapeutic effective amount of the compound, or the salt, stereoisomer or tautomer thereof according to claim 1 to the subject.
12 . The method of claim 11 , wherein the pain comprises chronic pain or neuropathic pain; depression comprises bipolar depression or major depressive disorder; and improving the cognitive function comprises preventing or treating Alzheimer's dementia or Parkinson's disease.
13 . A method for anesthesia, alleviating pain, improving cognitive function, lung protection, anti-depression, mitigating anxiety and post-traumatic stress syndrome, or preventing or treating amyotrophic lateral sclerosis or complex regional pain syndrome of a subject, comprising administrating a therapeutic effective amount of the compound, or the salt, stereoisomer or tautomer thereof according to claim 5 to the subject.
14 . The method of claim 13 , wherein the pain comprises chronic pain or neuropathic pain; depression comprises bipolar depression or major depressive disorder; and improving the cognitive function comprises preventing or treating Alzheimer's dementia or Parkinson's disease.