首页> 外国专利> Maleate salts of (E) -N- {4- 3-Chloro-4- (2-pyridinylmethoxy) anilino -3-cyano-7-ethoxy-6-quinolinyl} -4- (dimethylamino) -2-butenamide and its crystalline forms

Maleate salts of (E) -N- {4- 3-Chloro-4- (2-pyridinylmethoxy) anilino -3-cyano-7-ethoxy-6-quinolinyl} -4- (dimethylamino) -2-butenamide and its crystalline forms

机译:(E)-N- {4- [3-氯-3-(2-吡啶基甲氧基)苯胺基] -3-氰基-7-乙氧基-6-喹啉基} -4-(二甲基氨基)-2-丁烯酰胺的马来酸盐和它的结晶形式

摘要

A method for preparing (E) -N- {4- [3-chloro-4- (2-pyridinylmethoxy) anilino] -3-cyano-7-ethoxy-6-quinolinyl} -4- (dimethylamino) -2-butenamide partially hydrated as a maleate salt comprising the steps of: i) heating (E) -N- {4- [3-chloro-4- (2-pyridinylmethoxy) anilino] -3-cyano-7-ethoxy-6- quinolinyl} -4- (dimethylamino) -2-butenamide and maleic acid at 50 ° C-60 ° C in a water solution: n-propanol and keep the mixture at 50-60 ° C for a minimum of 15 min; ii) cooling said solution for at least one hour at 40 ° C and keeping the solution cooled to 40 ° C for 12 hours; iii) further cooling the cooled solution to room temperature, 25 ° C, for a minimum of 4 hours and keeping the solution further cooled to room temperature, 25 ° C, for at least 2 hours; iv) filter the mixture obtained in step iii) to obtain (E) -N- {4- [3-chloro-4- (2- pyridinylmethoxy) anilino] -3-cyano-7-ethoxy-6 maleate salt -quinolinyl} -4- (dimethylamino) -2-crystalline butenamide, where the (E) -N- {4- [3-chloro-4- (2-pyridinylmethoxy) anilino] -3-cyano-7 maleate salt -ethoxy-6-quinolinyl} -4- (dimethylamino) -2- crystalline butenamide is (E) -N- {4- [3-chloro-4- (2-pyridinylmethoxy) anilino] -3-cyano-7 maleate -ethoxy-6- quinolinyl} -4- (dimethylamino) -2-butenamide monohydrate; v) drying the (E) -N- {4- [3-chloro-4- (2-pyridinylmethoxy) anilino] -3-cyano-7-ethoxy-6-quinolinyl} -4- (dimethylamino) -2 maleate -butenamide monohydrate from step iv) under vacuum at a temperature above 30 ° C for 12 to 48 hours to obtain (E) -N- {4- [3-Chloro-4- (2-pyridinylmethoxy) anilino] maleate] -3-cyano-7-ethoxy-6- quinolinyl} -4- (dimethylamino) -2-butenamide anhydrous crystalline; and vi) exposing the (E) -N- {4- [3-chloro-4- (2-pyridinylmethoxy) anilino] -3-cyano-7-ethoxy-6-quinolinyl} -4- (dimethylamino) - maleate Anhydrous crystalline 2-butenamide at a relative humidity of 75% at room temperature (20-25 ° C) for 22 days, to form (E) -N- {4- [3-Chloro-4- (2-pyridinylmethoxy) maleate ) anilino] -3-cyano-7- ethoxy-6-quinolinyl} -4- (dimethylamino) -2-partially hydrated crystalline butenamide.
机译:(E)-N- {4- [3-氯-4-(2-吡啶基甲氧基)苯胺基] -3-氰基-7-乙氧基-6-喹啉基} -4-(二甲基氨基)-2-丁烯酰胺的制备方法作为马来酸盐部分水合,包括以下步骤:i)加热(E)-N- {4- [3-氯-4-(2-吡啶基甲氧基)苯胺基] -3-氰基-7-乙氧基-6-喹啉基} -4-(二甲基氨基)-2-丁烯酰胺和马来酸在50°C至60°C的水溶液中:正丙醇并将混合物在50-60°C保持至少15分钟; ii)在40°C下冷却所述溶液至少一小时,并保持溶液在40°C下冷却12小时; iii)将冷却的溶液进一步冷却至室温25°C至少4小时,并保持溶液进一步冷却至25°C室温至少2小时; iv)过滤步骤iii)中获得的混合物以获得(E)-N- {4- [3-氯-3-(2-吡啶基甲氧基)苯胺基] -3-氰基-7-乙氧基-6马来酸盐-喹啉基} -4-(二甲氨基)-2-结晶丁烯酰胺,其中(E)-N- {4- [3-氯-4-(2-吡啶基甲氧基)苯胺基] -3-氰基-7马来酸盐-乙氧基-6-喹啉基} -4-(二甲基氨基)-2-结晶丁烯酰胺是(E)-N- {4- [3-氯-4-(2-吡啶基甲氧基)苯胺基] -3-氰基-7马来酸酯-乙氧基-6-喹啉基} -4-(二甲氨基)-2-丁烯酰胺一水合物; v)干燥(E)-N- {4- [3-氯-4-(2-吡啶基甲氧基)苯胺基] -3-氰基-7-乙氧基-6-喹啉基} -4-(二甲氨基)-2马来酸酯-将步骤iv)中的丁烯酰胺一水合物在真空中于高于30℃的温度下保持12至48小时,以获得(E)-N- {4- [3- [3-氯-4-(2-吡啶基甲氧基)苯胺基]马来酸酯] -3-氰基-7-乙氧基-6-喹啉基} -4-(二甲基氨基)-2-丁烯酰胺无水晶体;和vi)暴露(E)-N- {4- [3-氯-4-(2-吡啶基甲氧基)苯胺基] -3-氰基-7-乙氧基-6-喹啉基} -4-(二甲氨基)-无水马来酸酯结晶的2-丁烯酰胺在相对湿度为75%的情况下在室温(20-25°C)下放置22天,形成(E)-N- {4- [3-Chloro-4-(2-吡啶基甲氧基)马来酸酯)苯甲基] -3-氰基-7-乙氧基-6-喹啉基} -4-(二甲基氨基)-2-部分水合的结晶丁烯酰胺。

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