CN110078729A - 一种水溶性氟苯尼考前药及其制备方法 - Google Patents

一种水溶性氟苯尼考前药及其制备方法 Download PDF

Info

Publication number
CN110078729A
CN110078729A CN201910503468.5A CN201910503468A CN110078729A CN 110078729 A CN110078729 A CN 110078729A CN 201910503468 A CN201910503468 A CN 201910503468A CN 110078729 A CN110078729 A CN 110078729A
Authority
CN
China
Prior art keywords
florfenicol
water
prodrug
solubility
preparation
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201910503468.5A
Other languages
English (en)
Inventor
史兰香
张宝华
陈东
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shijiazhuang University
Original Assignee
Shijiazhuang University
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Shijiazhuang University filed Critical Shijiazhuang University
Priority to CN201910503468.5A priority Critical patent/CN110078729A/zh
Publication of CN110078729A publication Critical patent/CN110078729A/zh
Pending legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/16Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
    • C07D295/20Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
    • C07D295/205Radicals derived from carbonic acid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/10Spiro-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/10Spiro-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/10Spiro-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

本发明公开了一种水溶性氟苯尼考前药及其制备方法。该类前药由单哌嗪季铵盐与固体光气和氟苯尼考缩合而成,具有充分的水溶性,在生理条件下该前药可以释放出氟苯尼考,发挥抗菌作用。

Description

一种水溶性氟苯尼考前药及其制备方法
技术领域
本发明涉及水溶性氟苯尼考前药及其制备方法,属于医药技术领域。
背景技术
氟苯尼考是一种专门用于动物保健的新型兽医用氯霉素类广谱抗菌药,是防治动物感染性疾病用量最大效果最好的抗菌药之一。但氟苯尼考水溶性很差,溶解速度缓慢,生物利用度低。原研商先灵-葆雅公司公开了氟苯尼考磷酸酯前药,其钠盐溶解度达700mg/mL,可以满足临床各种制剂要求(US2005/0182031和CN200480038867)。先灵-普劳公司通过氟苯尼考的仲羟基与带铵基团的化合物成碳酸酯或羧酸酯制备了高水溶性的氟苯尼考前药,并制成饮水剂和注射剂使用(CN200780051290.0)。Yerramill等氟苯尼考与丁二酸酐合成了氟苯尼考二酸单酯前药,产品水溶性好,可制成水针或粉针剂(US2005/0014828)。但是,对于其它有益特征的水溶性氟苯尼考仍然存在需求。
发明内容
本发明的目的在于提供一种水溶性氟苯尼考前药,其能在体内或生理条件下高速率的释放出氟苯尼考原药,发挥抗菌作用。
本发明的另一目的在于提供上述水溶性氟苯尼考前药的制备方法。
以下对本发明进行详细描述。
本发明提供的水溶性氟苯尼考前药为以下的任意一种:
本发明还提供了上述化合物的制备方法:
式中,n为1,2;
本发明的水溶性氟苯尼考前药,能在体内或生理条件下释放出氟苯尼考,发挥抗菌作用。
通过以下实施例进一步举例说明本发明,但应注意本发明的范围并不受这些实施例的任何限制。
具体实施方式
实施例1
化合物(1)的制备
将681mg(3mmol)3,6-二氮杂氮螺[5.5]壬烷氯化物盐酸盐(IIa)和690mg (5mmol)K2CO3加入到5mLDMF中,搅拌,冷却至0℃,慢慢加入297mg(1mmol)固体光气,搅拌40min,再滴加1.07g(3mmol)氟苯尼考的5mL DMF溶液,反应约40min,过滤除盐,滤液慢慢滴加适量的乙酸乙酯至浑浊,放置,析出固体,过滤,滤饼溶于乙醇中,过滤除盐,滤液慢慢滴加适量的乙酸乙酯至浑浊,放置,析出结晶,过滤,干燥,得到氟苯尼考前药化合物(1),收率92%。
实施例2
化合物(2)的制备
用636mg(3mmol)5,8-二氮杂氮螺[4.5]辛烷氯化物盐酸盐(IIb)代替681mg(3mmol)3,6-二氮杂氮螺[5.5]壬烷氯化物盐酸盐(IIa),其它操作同实施例1,得到氟苯尼考前药化合物(2),收率90%。
实施例3
化合物(3)的制备
用981mg(3mmol)3-氧-6,9-二氮杂氮螺[5.5]壬烷氯化物盐酸盐(IIc)代替681mg(3mmol)3,6-二氮杂氮螺[5.5]壬烷氯化物盐酸盐(IIa),其它操作同实施例1,得到氟苯尼考前药化合物(3),收率88%。
实施例4
化合物(4)的制备
用981mg(3mmol)3-(N,N-二甲基)氮-6,9-二氮杂氮螺[5.5]壬烷二氯化物盐酸盐(IId)代替681mg(3mmol)3,6-二氮杂氮螺[5.5]壬烷氯化物盐酸盐(IIa),其它操作同实施例1,得到氟苯尼考前药化合物(4),收率83%。
实施例5
化合物(5)的制备
用1.28g(3mmol)3-(N,N-二正丁基)氮-7,9-二氮杂氮螺[5.5]癸烷二氯化物盐酸盐(IIe)代替681mg(3mmol)3,6-二氮杂氮螺[5.5]壬烷氯化物盐酸盐(IIa),其它操作同实施例1,得到氟苯尼考前药化合物(5),收率81%。
实施例6
化合物(6)的制备
用642mg(3mmol)N,N-二乙基哌嗪季铵盐氯化物盐酸盐(IIf)代替681mg(3mmol)3,6-二氮杂氮螺[5.5]壬烷氯化物盐酸盐(IIa),其它操作同实施例1,得到氟苯尼考前药化合物(6),收率93%。
实施例7
氟苯尼考前药溶解释放性能测试
按药典方法测定室温(25±2℃)下各前药的溶解度(表1)。
在室温(25±2℃)下,将各前药分别配成1mg/mL浓度的水溶液,再分别分别精密量取1.0mL澄清的各前药的溶液加入到1.0mL pH1.2的盐酸溶液中,摇匀。从0分钟开始,每隔1分钟按药典规定的HPLC方法测定氟苯尼考的释放浓度,并计算氟苯尼考的释放速率(表1)。释放速率=氟苯尼考最高释放浓度/相应释放时间。

Claims (3)

1.一种水溶性氟苯尼考前药,其特征在于,所述水溶性氟苯尼考前药为以下的任意一种:
2.根据权利要求1所述的水溶性氟苯尼考前药,制备方法包括以下步骤:
式中,n为1,2;
3.根据权利要求1所述的一种水溶性氟苯尼考前药,其特征在于,它能在体内或生理条件下释放出氟苯尼考,发挥抗菌作用。
CN201910503468.5A 2019-06-11 2019-06-11 一种水溶性氟苯尼考前药及其制备方法 Pending CN110078729A (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910503468.5A CN110078729A (zh) 2019-06-11 2019-06-11 一种水溶性氟苯尼考前药及其制备方法

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910503468.5A CN110078729A (zh) 2019-06-11 2019-06-11 一种水溶性氟苯尼考前药及其制备方法

Publications (1)

Publication Number Publication Date
CN110078729A true CN110078729A (zh) 2019-08-02

Family

ID=67424070

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201910503468.5A Pending CN110078729A (zh) 2019-06-11 2019-06-11 一种水溶性氟苯尼考前药及其制备方法

Country Status (1)

Country Link
CN (1) CN110078729A (zh)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112194788A (zh) * 2020-09-15 2021-01-08 石家庄学院 一种水溶性氟苯尼考及其制备方法

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1897954A (zh) * 2003-12-23 2007-01-17 先灵-普劳有限公司 具有改善水溶性的氟苯尼考前药
CN101289416A (zh) * 2008-03-03 2008-10-22 西南大学 体内速释的高水溶性氟苯尼考前药
CN101337916A (zh) * 2008-08-12 2009-01-07 张家港市恒盛药用化学有限公司 氟苯尼考磺酸酯及其盐以及它们的制备方法
CN101605756A (zh) * 2006-12-13 2009-12-16 先灵-普劳有限公司 氟苯尼考及其类似物的水溶性前药
CN101993399A (zh) * 2009-08-10 2011-03-30 浙江康牧药业有限公司 一锅法制备氟苯尼考琥珀酸钠的方法
US20140275010A1 (en) * 2013-03-12 2014-09-18 Guo Zhu Zheng Quaternary salts

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1897954A (zh) * 2003-12-23 2007-01-17 先灵-普劳有限公司 具有改善水溶性的氟苯尼考前药
CN101605756A (zh) * 2006-12-13 2009-12-16 先灵-普劳有限公司 氟苯尼考及其类似物的水溶性前药
CN101289416A (zh) * 2008-03-03 2008-10-22 西南大学 体内速释的高水溶性氟苯尼考前药
CN101337916A (zh) * 2008-08-12 2009-01-07 张家港市恒盛药用化学有限公司 氟苯尼考磺酸酯及其盐以及它们的制备方法
CN101993399A (zh) * 2009-08-10 2011-03-30 浙江康牧药业有限公司 一锅法制备氟苯尼考琥珀酸钠的方法
US20140275010A1 (en) * 2013-03-12 2014-09-18 Guo Zhu Zheng Quaternary salts

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112194788A (zh) * 2020-09-15 2021-01-08 石家庄学院 一种水溶性氟苯尼考及其制备方法
CN112194788B (zh) * 2020-09-15 2022-08-02 石家庄学院 一种水溶性氟苯尼考及其制备方法

Similar Documents

Publication Publication Date Title
CN103694172A (zh) 含氮杂芳基化合物的衍生物
HU188181B (en) Process for producing salts of naphtiridine and quinoline compounds of antimicrobial activity
CN110078729A (zh) 一种水溶性氟苯尼考前药及其制备方法
KR100953271B1 (ko) 1-시클로프로필-6-플루오로-7-(8-메톡시이미노-2,6-디아자-스피로[3.4]옥트-6-일)-4-옥소-1,4-디히드로-[1,8]나프티리딘-3-카르복실산 아스파르트산 염, 이의 제조방법 및 이를포함하는 항균용 약학 조성물
WO1995028407A1 (de) Lobaplatin-trihydrat
CN104447541A (zh) 博舒替尼化合物
CN102234265A (zh) 兰索拉唑化合物
CN102198134B (zh) 一种新型稳定的尤利沙星盐酸盐在制备抗感染药物中的应用
CN103222975B (zh) 恩诺沙星盐在制备猪用口服制剂中的应用
CN105534937A (zh) 一种头孢羟氨苄片剂及其制备方法
CN104095847A (zh) 一种包含亚胺培南西司他丁钠的药物组合物及其制剂
PL214849B1 (pl) Tetrahydrat soli kwasu benzochinolizyno-2-karboksylowego z arginina, sposób jego wytwarzania, kompozycja zawierajaca przedmiotowy tetrahydrat soli oraz jego zastosowanie
CN102574840B (zh) R-7-(3-氨甲基-4-甲氧基亚氨基-3-甲基-吡咯烷-1-基)-1-环丙基-6-氟-4-氧代-1,4-二氢-[1,8]萘啶-3-羧酸l-天冬氨酸盐及其制备方法以及包含该盐的抗菌用药学组合物
WO2017096907A1 (zh) 一种噁唑烷酮类抗菌药物钠盐的晶型a及其制备方法和应用
ES2846735T3 (es) Solvato metanólico de sulfato de morfina, procedimientos para hacer el mismo y las composiciones relacionadas y métodos de tratamiento del dolor
DE1806926A1 (de) Lithiumsalz der Hydrochinonsulfonsaeure
CN103483315A (zh) 7-(3-氨甲基-4-烷氧亚胺基-1-吡咯烷基)-1-[(1r,2s)-2-氟环丙基]喹诺酮羧酸类化合物及其制备方法
CN114230454B (zh) 没食子酸类天然活性成分的钙配合物及其合成方法和应用
CN110041347A (zh) 头孢唑啉钠新化合物及其组合物和用途
CN101181271A (zh) 门冬氨酸喹诺酮类抗菌药物水溶性盐及其注射剂型
CN106188072A (zh) 氘代4-[(3-乙炔苯基)氨基]-6,7-苯-12冠-4-喹唑啉衍生物以及包含该衍生物的药物组合物
CN110950910A (zh) 一种稳定的米诺膦酸化合物
CN103965189B (zh) 一种新的盐酸莫西沙星化合物
CN102020660A (zh) 一种安妥沙星盐酸盐结晶形式、其制备方法和包含它的药物组合物
CN115873068A (zh) 甘氨酰谷氨酰胺锌络合物及其制备方法和应用

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
WD01 Invention patent application deemed withdrawn after publication
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20190802