US2017001981A1PendingUtilityA1
Sulfonyl amide derivatives for the treatment of abnormal cell growth
Est. expiryApr 18, 2027(~0.8 yrs left)· nominal 20-yr term from priority
Inventors:Michael Joseph LuzzioKevin Daniel Freeman-CookSamit Kumar BhattacharyaMatthew Merrill HaywardCatherine Angela HulfordChristopher Lowell AutryXumiao ZhaoJun XiaoKendra Louise Nelson
A61P 43/00A61P 35/02A61P 35/00A61P 35/04A61P 29/00A61P 25/00A61P 27/02A61P 17/06A61P 19/02A61P 19/10A61P 13/08A61P 19/08C07D 403/12C07D 401/14C07D 401/12C07D 417/14C07D 475/00C07D 417/12C07D 413/14C07D 239/48C07D 241/20C07D 405/14A61K 31/506A61K 31/505
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Claims
Abstract
The present invention relates to a compound of the formula I wherein R 1 to R 6 , A, B, n and m are as defined herein. Such novel sulfonyl amide derivatives are useful in the treatment of abnormal cell growth, such as cancer, in mammals. This invention also relates to a method of using such compounds in the treatment of abnormal cell growth in mammals, especially humans, and to pharmaceutical compositions containing such compounds.
Claims
exact text as granted — not AI-modifiedWe claim:
1 . A method of making a compound of Formula (1), or a pharmaceutically acceptable salt thereof, the method comprising:
reacting a compound of Formula (C3):
with a compound of Formula (B5):
thereby providing the compound of Formula (1), or a pharmaceutically acceptable salt thereof.
2 . The method of claim 1 , wherein the reaction of the compound of Formula (C3) and the compound of Formula (B5) is performed in the presence of a base.
3 . The method of claim 2 , wherein the base is diethylamine (DIEA).
4 . The method of claim 1 , wherein the reaction of the compound of Formula (C3) and the compound of Formula (B5) is performed for 20 hours.
5 . The method of claim 1 , wherein the reaction is performed in the presence of a solvent.
6 . The method of claim 5 , wherein the solvent is 1,2-dichloroethane (DCE):t-BuOH.
7 . The method of claim 6 , wherein the 1,2-dichloroethane (DCE):t-BuOH is 1:1 vol:vol.
8 . The method of claim 1 , wherein the temperature is 80° C.
9 . The method of claim 1 , wherein isolating the compound of Formula (1) comprises decreasing the temperature of the reaction mixture to ambient temperature.
10 . The method of claim 9 , wherein the temperature is 25° C.
11 . The method of claim 9 , wherein isolating the compound of Formula (1) comprises treating the reaction of the compound of Formula (C3) and the compound of Formula (B5) with EtOAc.
12 . The method of claim 9 , wherein the reaction of the compound of Formula (C3) and the compound of Formula (B5) is washed with water.
13 . The method of claim 9 , wherein the reaction of the compound of Formula (C3) and the compound of Formula (B5) is dried over MgSO 4 .
14 . The method of claim 9 , wherein isolating the compound of Formula (1) comprises filtration.Cited by (0)
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