Key intermediate for synthesis of prostaglandin compound and preparation method thereof
The present invention relates to the technical field of organic chemical engineering, and in particular to a key intermediate for synthesizing prostaglandin compounds and a preparation method therefor. When applied to the synthesis of prostaglandin compounds, the process flow is simplified, the yield and product purity are improved, the production costs are reduced, and the industrial application is easy.
1 . A key intermediate for synthesis of a prostaglandin compound, having a structure shown below:
wherein denotes a single bond or double bond, and if it is a double bond, R 1 is absent; and wherein R 1 and R 2 are each H or protecting groups; R 3 and R 4 are the same or different alkyl or aryl, or R 3 and R 4 form a ring.
2 . The key intermediate for the synthesis of the prostaglandin compound according to claim 1 , having a structure shown below:
wherein R 1 , R 2 , R 3 , and R 4 are as defined above.
3 . The key intermediate for the synthesis of the prostaglandin compound according to claim 1 , which is
wherein R 1 , R 2 , R 3 , and R 4 are as defined above.
4 . The key intermediate for the synthesis of the prostaglandin compound according to claim 1 , which is
wherein R 1 and R 2 are as defined above, and n is an integer from 1 to 3.
5 . The key intermediate for the synthesis of the prostaglandin compound according to claim 1 , wherein the intermediate is
6 . The key intermediate for the synthesis of the prostaglandin compound according to claim 1 , wherein the protecting group is selected from an ether protecting group, an acyl protecting group, a silyl ether protecting group, an acetal protecting group.
7 . The key intermediate for the synthesis of the prostaglandin compound according to claim 1 , wherein the intermediate is selected from:
8 . A method for preparing the key intermediate for the synthesis of the prostaglandin compound according to claim 1 , comprising steps of:
a) asymmetrically reducing compound S1 to obtain chiral alcohol compound S2, and then protecting hydroxyl group of the chiral alcohol compound S2 with silane to obtain Weinreb amide compound S3;
b) subjecting the Weinreb amide compound S3 to an addition reaction with an alkyne reagent to obtain enyne compound S4;
c) subjecting the enyne compound S4 to a Zhang enyne cycloisomerization to obtain five-membered ring S5;
d) conjugating the five-membered ring S5 to reduce double bond thereof to obtain compound S6, and further reducing ketone of the compound S6 to obtain compound S7; and
e) deprotecting the compound S7 by removing TIPS thereof to obtain compound S8;
referring to the following reaction route:
9 . The key intermediate for the synthesis of the prostaglandin compound according to claim 1 , having a structure shown below:
wherein R 1 , R 2 , R 3 , and R 4 are as defined above.
10 . The key intermediate for the synthesis of the prostaglandin compound according to claim 1 , which is
wherein R 1 , R 2 , R 3 , and R 4 are as defined above.
11 . The key intermediate for the synthesis of the prostaglandin compound according to claim 1 , which is
wherein R 1 and R 2 are as defined above, and n is an integer from 1 to 3.
12 . The key intermediate for the synthesis of the prostaglandin compound according to claim 1 , wherein the intermediate is selected from:
wherein P is a protecting group.