相似化合物
34839-14-0 62037-46-1 53494-57-8欧盟法规
C&L通报上下游产品
3-benzylidenamino-1-chloropropan-2-ol 2-(3-chloro-2-hydroxypropyl)-1H-isoindole-1,3(2H)-dione epichlorohydrin (S)(E,Z)-1-(benzylideneamino)-3-chloropropan-2-ol tert-butyl-3-chloro-2-hydroxypropylcarbamate N-[(2S)-3-chloro-2-hydroxypropyl]-5-chlorothiophene-2-carboxamide tert-butyl (2S)-3-chloro-2-hydroxypropylcarbamate rac-1-acetamido-2-acetoxy-3-chloropropane (S)-1-Benzalimino-3-Chloro-2-Propanol置于盐酸体系中,用 水,甲苯 用作溶剂,化学反应 3.5H,反应生成(S)-1-氨基-3-氯-2-丙醇盐酸盐
参考文献:Synthesis And In Vitro Antibacterial Activity Of Novel Fluoroalkyl-Substituted Pyrazolyl Oxazolidinones
标题:Synthesis And In Vitro Antibacterial Activity Of Novel Fluoroalkyl-Substituted Pyrazolyl Oxazolidinones
摘要:一系列新颖的含氟烷基取代的吡唑并含有噁唑烷酮衍生物被合成并对其抗菌活性进行评估,针对六种革兰氏阳性细菌病原体.大多数具有非常好的抗菌活性,其中三种与利奈唑齐相当.
Doi:10.1039/c5Ra11782H
海关参考信息
- 2905122000-异丙醇
2905590020-2-氯乙醇
2922110001-单乙醇胺
2903110000-一氯甲烷及氯乙烷 - 💡 提示:海关信息按照顺序优先匹配,如需确认的海关信息,请参考相关资料。
- 详情请参考:📖 海关编码查询和海关进出口税则
专利信息
专利号:WO-2013046211-A1
优先权日:2011-09-27
标 题 :Processes for the preparation of 5-chloro-n-({(5s)-2-oxo-3-[4-(3-oxo-4-morpholinyl) phenyl]-1,3-oxazolidin-5-yl}methyl)-2-thiophene-carboxamide and intermediates thereof
发明人:MOHAN RAO DODDA; KRISHNA REDDY PINGILI; VENKAT REDDY BUTHUKURI
权利人:SYMED LABS LTD; MOHAN RAO DODDA; KRISHNA REDDY PINGILI; VENKAT REDDY BUTHUKURI
摘要:TThe present invention provides processes for the preparation of 5-chloro-N-({(5S)-2-oxo-3-[4-(3-oxo-4-morpholinyl)phenyl]-1,3-oxazolidin-5-yl}methyl)-2-thiophene-carboxamide (I) and intermediates thereof. Also provides novel intermediates and their use in the synthesis of oxazolidine derivatives.
专利号:US-2025066340-A1
优先权日:2021-11-17
标题 :Method for synthesizing rivaroxaban
发明人:HU JIAXING; ZHANG JIAN; ZHANG HAO; ZHU ZHENGHE; WANG ANYU; HUANG WENFENG; ZHU YAN; JIN YONGJUN
权利人:ZHEJIANG HUAHAI PHARM CO LTD; ZHEJIANG HUAHAI LICHENG PHARMACEUTICAL CO LTD
摘要:Provided in the present invention is a method for synthesizing rivaroxaban. The method comprises: reacting an intermediate I with an intermediate II in an organic solvent in the presence of an alkali to obtain rivaroxaban, wherein the synthesis route is shown as follows, R in formula I is phenyl or substituted phenyl, and in substitution, the substituent is selected from nitro, halogen and C 1 -C 6 alkyl; and X in formula II is bromine or chlorine. The method for synthesizing rivaroxaban provided in the present invention is short in terms of route, mild in terms of reaction conditions, simple in terms of post-treatment, high in terms of reaction yield and very suitable for industrial production
专利号:CN-116789557-A
优先权日:2023-05-31
标题:Synthesis method of (S) -1-amino-3-chloro-2-propanol hydrochloride