مولانا مفتی سید عبدالرحیم لاجپوری
علمی حلقوں میں یہ خبر بڑے افسوس کے ساتھ سنی گئی کہ ۱۸؍ نومبر ۲۰۰۱ء کو مولانا عبدالرحیم لاجپوری رحلت فرماگئے، وہ گجرات ہی نہیں اس برصغیر کے ممتاز اور جید عالم دین تھے، فقہ و فتاویٰ پر ان کی نظر بڑی گہری اور وسیع تھی، علم راسخ اور فقہ و افتا میں کامل الفن ہونے کے ساتھ ورع و تقوی اور سیرت و اخلاق کی پاکیزگی میں بھی سلف صالحین کا نمونہ تھے۔
مفتی صاحب ایک سید گھرانے کے چشم و چراغ تھے، ان کا سلسلہ نسب ستائیسویں پشت میں حضرت شیخ عبدالقادر جیلانیؒ سے جاملتا ہے، ان کا آبائی وطن گجرات میں لاجپور تھا لیکن ان کی پیدائش ضلع گجرات کے مشہور شہر بلسار کے قصبہ نوساری میں دسمبر ۱۹۰۳ء؍ شوال ۱۳۲۱ھ میں ہوئی، اپنے دادا مولانا سید ابراہیم صاحب سے تعلیم شروع کی تھی کہ ان کا انتقال ہوگیا، جس کے بعد والد مولانا سید عبدالکریم صاحب اور چچا حافظ سید حسام الدین صاحب سے حفظِ قرآن کی تکمیل کی، قرأت و تجوید میں بڑا کمال حاصل کیا، قرآن مجید بہت اچھا پڑھتے تھے، آواز میں بڑی تاثیر اور لہجہ نہایت دلکش تھا، اس لیے طالب علمی ہی کے زمانے میں نوساری کی جامع مسجد کے امام ہوگئے لیکن جلد ہی قدردانوں نے راندیر بلالیا اور وہاں کی جامع مسجد کا امام مقرر کردیا۔
مدرسہ محمدیہ عربیہ جامعہ حسینیہ راندیر میں درسیات کی تکمیل کی اور یہیں درس و تدریس کی خدمت پر مامور ہوئے، طالب علمی میں فقہ و افتا سے خاص شغف ہوگیا تھا اور اسی زمانے سے اپنے اساتذہ کی رہنمائی میں فتاوی لکھنا شروع کردیا تھا، جس کا سلسلہ مدۃ العمر جاری رہا ۔ اس کی وجہ سے ملک میں معتبر فقیہ و مفتی کی حیثیت سے مشہور ہوئے اور کئی جلدوں میں...
As well as per Shariah, it is admissible and some of the time even mandatory to save the devotees from the activities that might lead them towards the prohibited exercises. Consequently, the decision of denial from these kinds of exercises is called Sadd-e-Zaree'a. This is the guideline derived from the Quran and Sunnah. As Almighty Allah prohibited the devotees to say 'Raina' because this word was utilized by Jews purposely in an off-base way with underhanded aims, while, Muslims introduced their solicitations by this equivalent word in the most elevated court of The Holy Prophet (harmony and gifts arrive) for looking for effortlessness and unwinding in their concerned issues. As in Quran: O People who Believe, don't tell (the Prophet Mohammed-harmony and gifts arrive), "Raina (Be accommodating towards us)" however say, "Unzurna (Look leniently upon us)", and listen mindfully in any case. [Baqarah 2:104]. (To disregard the Holy Prophet - harmony and endowments arrive - is impiety.) Ibn Hazm in his famous book Al-Aḥkām Fī ūṣūl Al-Aḥkām has objected to the mentioned verse from which jurists have taken the argument of Sadd-e-Zaree'a. Because the Zahiri school of thought is based on the appearance of the text (Quran o Hadees). This is why Ibn Hazm Zahiri denies it (the source of Shariah), and proves that accepting the source of Shariah is an increase in religion which is in itself illegitimate as well as the opposition of the Prophet (peace and blessings of Allah be upon him). There is also the addition of items by their thoughts in Shariah. In the above article, an analytical study of the objections of Allama Ibn Hazm will be presented, explaining the sources and the arguments as to whether or not their source is Shariah.
In the present workpyrimido[5,4-c]quinoline-2,4(1H,3H)-diones (5-24) were synthesized by two step reaction sequence involving Knoevenagel condensation and Doebner Miller reaction. Compounds (5-24) were availed by fusion of Knoevenagel adducts (5benzylidenepyrimidine-2,4,6(1H,3H,5H)-trione and 5-(3-nitrobenzylidene)pyrimidine2,4,6(1H,3H,5H)-trione) (3a-b) with anilines viz.sulfanilamide, 4-amino-N-(thiazol-2yl)benzenesulfonamide, sulfamethazine, sulfaguanidine, sulfamethoxazole, paminobenzoic acid, p-nitroaniline, 3-nitroaniline, 3-hydroxyaniline, p-phenylaniline, 5amino-2-hydroxybenzoic acid, 3-aminoacetophenone, 4-amino-2-hydroxybenzoic acid, 4aminoacetophenone and 4-chloroaniline (4a-o) in an oil bath at 170-265 oCafforded desired compounds in moderate to good yields (55-74%). All the compounds were tediously characterized. The prepared compounds (5-19) were tested for their in vitro antioxidant activity and at all instances they exhibited excellent activity in comparison to control Ascorbic acid. Compounds (20-24) were selectively screened for in vitro antibacterial and antiviral activities as these compounds has active pharmacophores in the structure. The most active compounds were 23, 21 and 22 having MIC 0.5, 1.25 and 1.75 µg respectively against P. vulgaris where ampicillin (MIC 2.25 µg) was employed as positive control. In case K. pneumonia compound 24 was found most active (MIC 0.1 µg) in comparison to control ampicillin (MIC 1.25 µg). In case of antiviral activity of the synthesized compounds (2024), compound (23) has expressed maximum in ovo antiviral potency against all four viruses (AIVH9N2, NDV, IBDV and IBV) with IC50 (0.001 µM). In case of synthesis of oxepines (38, 38´, 43 and 43´), a multi-step strategy (9 steps) is developed starting from 1-indanone anf finally the more polar compound 38 was dyrolysed to compound (40) to avail above mentioned compounds in respectable overall yield (0.39%).