【药物名称】STX-237
化学结构式(Chemical Structure):
参考文献No.61773
标题:Steroidal cpds. for inhibiting steroid sulphatase
作者:Reed, M.J.; Potter, B.V.L.; Woo, L.W.L. (Sterix Ltd.)
来源:WO 0333518
合成路线图解说明:

The oxidation of 3-(benzyloxy)estrone (I) with I2 and KOH in refluxing methanol gives 3-(benzyloxy)-16,17-seco-estra-1,3,5(10)-triene-16,17-dioic acid (II), which is cyclized with urea at 180篊 to yield the cyclic imide (III). The alkylation of (III) with propyl chloride (IV) and NaH in DMF affords the N-propyl derivative (V). Alternatively, the N-propyl derivative (V) can also be obtained by direct cyclization of diacid (II) with propylamine (VI) at 180?C. The debenzylation of (V) to the 3-hydroxy derivative (VII) is performed by hydrogenation with H2 over Pd/C in methanol/THF. Finally, compound (VII) is treated with chlorosulfonamide and NaH in DMF to provide the target sulfamate.

合成路线图解说明:

The oxidation of 3-(benzyloxy)estrone (I) with I2 and KOH in refluxing methanol gives 3-(benzyloxy)-16,17-seco-estra-1,3,5(10)-triene-16,17-dioic acid (II), which is cyclized with urea at 180?C to yield the cyclic imide (III). The alkylation of (III) with 3-(chloromethyl)pyridine (IV) and NaH in DMF affords the N-(3-pyridylmethyl) derivative (V). Alternatively, the N-(3-pyridylmethyl) derivative (V) can also be obtained by direct cyclization of diacid (II) with 3-pyridylmethylamine (VI) at 180?C. The debenzylation of (V) to the 3-hydroxy derivative (VII) is performed by hydrogenation with H2 over Pd/C in methanol/THF. Finally, compound (VII) is treated with chlorosulfonamide and NaH in DMF to provide the target sulfamate.

参考文献No.62368
标题:Use
作者:Reed, M.J.; Potter, B.V.L. (Sterix Ltd.)
来源:WO 0232409
合成路线图解说明:

1) 4-Chloro-2'-bromoacetophenone (I) is condensed with 2-amino 5-chloropyridine (II) to give 6-chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridine (III). 2) The above compound is reacted with formaldehyde and dimethylamine under Mannich conditions affording the 3-dimethylaminomethyl derivative (IV), which is subsequently quaternized with methyl iodide to afford the quaternary iodide (V). 3) Displacement of trimethylamine from salt (V) with cyanide ion leads to formation of the nitrile (VI), which on hydrolysis with hydrochloric acid in acetic acid gives the corresponding acid (VII). 4) In situ conversion of the acid to its acid chloride with phosphorus oxychloride followed by treatment with di-n-propylamine then leads to alpidem.

合成路线图解说明:

The oxidation of 3-(benzyloxy)estrone (I) with I2 and KOH in refluxing methanol gives 3-(benzyloxy)-16,17-seco-estra-1,3,5(10)-triene-16,17-dioic acid (II), which is cyclized with urea at 180篊 to yield the cyclic imide (III). The alkylation of (III) with propyl chloride (IV) and NaH in DMF affords the N-propyl derivative (V). Alternatively, the N-propyl derivative (V) can also be obtained by direct cyclization of diacid (II) with propylamine (VI) at 180?C. The debenzylation of (V) to the 3-hydroxy derivative (VII) is performed by hydrogenation with H2 over Pd/C in methanol/THF. Finally, compound (VII) is treated with chlorosulfonamide and NaH in DMF to provide the target sulfamate.

合成路线图解说明:

The oxidation of 3-(benzyloxy)estrone (I) with I2 and KOH in refluxing methanol gives 3-(benzyloxy)-16,17-seco-estra-1,3,5(10)-triene-16,17-dioic acid (II), which is cyclized with urea at 180?C to yield the cyclic imide (III). The alkylation of (III) with 3-(chloromethyl)pyridine (IV) and NaH in DMF affords the N-(3-pyridylmethyl) derivative (V). Alternatively, the N-(3-pyridylmethyl) derivative (V) can also be obtained by direct cyclization of diacid (II) with 3-pyridylmethylamine (VI) at 180?C. The debenzylation of (V) to the 3-hydroxy derivative (VII) is performed by hydrogenation with H2 over Pd/C in methanol/THF. Finally, compound (VII) is treated with chlorosulfonamide and NaH in DMF to provide the target sulfamate.

参考文献No.727400
标题:D-ring modified estrone derivatives as novel potent inhibitors of steroid sulfatase
作者:Fischer, D.S.; Woo, L.W.L.; Mahon, M.F.; Purohit, A.; Reed, M.J.; Potter, B.V.L.
来源:Bioorg Med Chem 2003,11(8),1685
合成路线图解说明:

The oxidation of 3-(benzyloxy)estrone (I) with I2 and KOH in refluxing methanol gives 3-(benzyloxy)-16,17-seco-estra-1,3,5(10)-triene-16,17-dioic acid (II), which is cyclized with urea at 180篊 to yield the cyclic imide (III). The alkylation of (III) with propyl chloride (IV) and NaH in DMF affords the N-propyl derivative (V). Alternatively, the N-propyl derivative (V) can also be obtained by direct cyclization of diacid (II) with propylamine (VI) at 180?C. The debenzylation of (V) to the 3-hydroxy derivative (VII) is performed by hydrogenation with H2 over Pd/C in methanol/THF. Finally, compound (VII) is treated with chlorosulfonamide and NaH in DMF to provide the target sulfamate.

合成路线图解说明:

The oxidation of 3-(benzyloxy)estrone (I) with I2 and KOH in refluxing methanol gives 3-(benzyloxy)-16,17-seco-estra-1,3,5(10)-triene-16,17-dioic acid (II), which is cyclized with urea at 180?C to yield the cyclic imide (III). The alkylation of (III) with 3-(chloromethyl)pyridine (IV) and NaH in DMF affords the N-(3-pyridylmethyl) derivative (V). Alternatively, the N-(3-pyridylmethyl) derivative (V) can also be obtained by direct cyclization of diacid (II) with 3-pyridylmethylamine (VI) at 180?C. The debenzylation of (V) to the 3-hydroxy derivative (VII) is performed by hydrogenation with H2 over Pd/C in methanol/THF. Finally, compound (VII) is treated with chlorosulfonamide and NaH in DMF to provide the target sulfamate.

参考文献No.729521
标题:Novel D-ring modified steroid derivatives as potent, non-estrogenic, steroid sulfatase inhibitors with in vivo activity
作者:Fischer, D.S.; Chander, S.K.; Woo, L.W.L.; Fenton, J.C.; Purohit, A.; Reed, M.J.; Potter, B.V.L.
来源:J Steroid Biochem Mol Biol 2003,84(2-3),343
合成路线图解说明:

The oxidation of 3-(benzyloxy)estrone (I) with I2 and KOH in refluxing methanol gives 3-(benzyloxy)-16,17-seco-estra-1,3,5(10)-triene-16,17-dioic acid (II), which is cyclized with urea at 180篊 to yield the cyclic imide (III). The alkylation of (III) with propyl chloride (IV) and NaH in DMF affords the N-propyl derivative (V). Alternatively, the N-propyl derivative (V) can also be obtained by direct cyclization of diacid (II) with propylamine (VI) at 180?C. The debenzylation of (V) to the 3-hydroxy derivative (VII) is performed by hydrogenation with H2 over Pd/C in methanol/THF. Finally, compound (VII) is treated with chlorosulfonamide and NaH in DMF to provide the target sulfamate.

合成路线图解说明:

The oxidation of 3-(benzyloxy)estrone (I) with I2 and KOH in refluxing methanol gives 3-(benzyloxy)-16,17-seco-estra-1,3,5(10)-triene-16,17-dioic acid (II), which is cyclized with urea at 180?C to yield the cyclic imide (III). The alkylation of (III) with 3-(chloromethyl)pyridine (IV) and NaH in DMF affords the N-(3-pyridylmethyl) derivative (V). Alternatively, the N-(3-pyridylmethyl) derivative (V) can also be obtained by direct cyclization of diacid (II) with 3-pyridylmethylamine (VI) at 180?C. The debenzylation of (V) to the 3-hydroxy derivative (VII) is performed by hydrogenation with H2 over Pd/C in methanol/THF. Finally, compound (VII) is treated with chlorosulfonamide and NaH in DMF to provide the target sulfamate.

Drug Information Express,Drug R&D,Chemical Database,Patent Search.
Copyright © 2006-2024 Drug Future. All rights reserved.Contact Us