CAS: 1192-63-8; 1-Pyrrolidinecarbonylchloride

该化合物是有机合成和制药应用中常用的一种活性丙烯衍生物,其关键优势在于它能够成为多用途建筑块,将丙烯-1-碳基分子引入目标分子中,便利形成氨化物,酯和其他功能化化合物.该化合物具有高反应性,在温和条件下能够高效地组合反应.在受控储存条件下的稳定性确保了合成工作流程的可靠处理.由于丙烯-1-碳基氯化物在药用化学中具有特别宝贵的价值,因为丙烯环在药用活性化合物中的流行.妥善处理预防措施由于其湿度敏感度和潜在腐蚀性,至关重要.

结构式图片

相似化合物

3760-54-1 20266-00-6 4030-18-6

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

CAS号123-75-1 四氢吡咯 | CAS号75-44-5 光气 | CAS号5470-26-8 1-Pyrrolidineca... | CAS号56475-80-0 吡咯烷甲基氨基甲酸酯 | CAS号29897-82-3 1-苄基吡咯烷 | CAS号32315-10-9 三光气 | CAS号81759-25-3 1,1''-羰基二吡咯烷 | CAS号60419-23-0 (R)-(-)-1-(2-吡咯... | CAS号720693-06-1 1-(2-氯-4-吡啶基羰基)吡咯烷 | CAS号144243-45-8 (9CI)-1-[(2R)-2... | CAS号62939-01-9 pyridin-3-yl py...

合成工艺路线路线简述

    1-吡咯烷羧酸乙酯置于三氯氧磷体系中,用 乙腈 用作溶剂,化学反应 2.0H,以64%的收率获得1-吡咯烷羰酰氯
    参考文献:Hoshino,Osamu; Saito,Keiji; Ishizaki,Miyuki,Synthetic Communications,1987,Vol. 17,# 16,P. 1887-1892
    标题:Hoshino,Osamu; Saito,Keiji; Ishizaki,Miyuki,Synthetic Communications,1987,Vol. 17,# 16,P. 1887-1892

    海关参考信息

    专利信息


    专利号:WO-2024185775-A1
    优先权日:2023-03-06
    标 题:Long-chain alkenyloxy–substituted benzoyl derivative and oligonucleotide synthesis method using same
    发明人:OKADA YOHEI; INANAGA KAZATO; SHOJI Yukiya; MIZUFUNE HIDEYA; SUDO TATSUYA; ADACHI Sota; HOSOI Kazushi
    权利人:SPERA PHARMA INC; TOKYO UNIV OF AGRICULTURE AND TECHNOLOGY
    摘要:The purpose of the present invention is to provide a novel pseudo–solid phase protecting group that can be used in liquid-phase oligonucleotide synthesis. The purpose of the present invention is also to provide an oligonucleotide synthesis method that uses a novel pseudo–solid phase protecting group. The present invention provides a compound represented by formula (1) (in which R represents a C14–60 alkenyl group, n represents 2 or 3, m represents 0 or 1, p represents 1 or 2, X represents C, N, O, or S, Y represents a single bond or B(CH 2 ) t * or may form a ring with X, and Z represents a single bond or (CH 2 ) s (s being an integer from 1 to 5)). The present invention also provides an oligonucleotide production method that uses the compound.

    专利号:WO-2022220019-A1
    优先权日:2021-04-16
    标题 :Long-chain dna synthesis using non-natural base
    发明人:MASAKI YOSHIAKI
    权利人:TOKYO INST TECH
    摘要:The purpose of the present invention is to provide a method for synthesizing a long-chain nucleic acid (particularly DNA) with high accuracy. The present invention provides a method for synthesizing a long-chain nucleic acid, the method comprising using: (i) a nucleoside-3'-O-phosphoramidite derivative having a non-natural nucleic acid base; or (ii) a nucleoside-3'-O-phosphoramidite derivative having a non-natural nucleic acid base and a nucleoside-3'-O-phosphoramidite derivative having a natural nucleic acid base in the chemical synthesis of a nucleic acid based on the phosphoramidite method.

    专利号:WO-2025082632-A1
    优先权日:2023-10-16
    标 题:Method and composition for oligonucleotide synthesis
    发明人:SAITO MASAHARU
    权利人:BACHEM HOLDING AG
    摘要:The invention pertains to a method for the synthesis of oligonucleotides using pseudo solid-phase protecting groups, wherein said method comprises a step of subjecting a solution comprising a component (C-0)# to one or more aqueous extractions, wherein the organic phase comprises the component (C-0)#. Said component (C-0)# is a nucleoside or an oligonucleotide, which is covalently bonded to a pseudo solid-phase protecting group and comprises a free backbone hydroxyl group. The aqueous phase of each of said one or more aqueous extractions has a pH-value in the range of 4-7.

    专利号:EP-4605403-A1
    优先权日:2022-10-17
    标 题:Method and composition for oligonucleotide synthesis
    发明人:SAITO MASAHARU; TAKEDA KAZUTAKA; OKADA YOHEI; LUTHER ANATOL
    权利人:BACHEM HOLDING AG
    摘要:The invention pertains to methods for the synthesis of oligonucleotides using pseudo solid-phase protecting groups, wherein said method comprises at least one aqueous extraction carried out in the presence of one or more amide solvents SA, wherein each amide solvent SA is an amide solvent comprising one or more alkyl groups, wherein these one or more alkyl groups together comprise in total 6−24 carbon atoms. The invention further pertains to compositions comprising an oligonucleotide which is covalently bonded to a pseudo solid-phase protecting group and a mixed solvent comprising on or more of the aforementioned amide solvents SA.

    专利号:WO-2024061842-A1
    优先权日:2022-09-19
    标 题:Improved oligonucleotide synthesis
    发明人:CREUSEN GUIDO; MINUTH MARCO; SAMSON DANIEL
    权利人:BACHEM HOLDING AG
    摘要:A method for the solid-phase synthesis of a target oligonucleotide OT is disclosed, wherein said method comprises a step of incubating a nucleoside or oligonucleotide, which is covalently linked to a solid support and comprises a backbone hydroxyl moiety protected by a di(p-methoxyphenyl)phenylmethyl (DMT) protecting group, with a deprotection mixture, thereby cleaving said protecting group from said nucleoside or oligonucleotide, wherein said deprotection mixture is a liquid composition comprising a solvent, a protic acid having a pKa equal to or smaller than 4, and at least one alcohol of Formula (D), wherein in RD-1 R,D-2 R,D-3 RD-4 and RD-5 are indepently of each other selected from the group consisting of H, OH, a e1-e6-alkyl group, O(C1-C6-aIkyl), C(O)(Ci-C6-alkyl), C(O)O(Ci-C6-alkyl), F, Cl, Br, I, and CN. Such a method does not only suppress depurination, but also results in an acceptable product yield.

    专利号:WO-2024083746-A1
    优先权日:2022-10-17
    标 题 :Method and composition for oligonucleotide synthesis
    发明人:SAITO MASAHARU; TAKEDA KAZUTAKA; OKADA YOHEI; LUTHER ANATOL
    权利人:BACHEM HOLDING AG
    摘要:The invention pertains to methods for the synthesis of oligonucleotides using pseudo solid-phase protecting groups, wherein said method comprises at least one aqueous extraction carried out in the presence of one or more amide solvents SA, wherein each amide solvent SA is an amide solvent comprising one or more alkyl groups, wherein these one or more alkyl groups together comprise in total 6−24 carbon atoms. The invention further pertains to compositions comprising an oligonucleotide which is covalently bonded to a pseudo solid-phase protecting group and a mixed solvent comprising on or more of the aforementioned amide solvents SA.
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    合成参考文献


    参考文献:10.1007/s00044-024-03250-y
    摘要:Liu Z, Li X, Huang M, Su Z, Zhang Q, Li Y, Zhou Y, Yu L, Liu W, Sang Z. Development of novel fluoro-substituted rivastigmine derivatives as selective AChE inhibitors for the treatment of AD. Med Chem Res. 2024 Jun 14;33(7):1195–204. doi: 10.1007/s00044-024-03250-y.
    参考文献:10.1007/s10637-008-9205-5
    摘要:Benaka Prasad SB, Vinaya K, Ananda Kumar CS, Swarup S, Rangappa KS. Synthesis of novel 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole derivatives as antiproliferative agents: a structure-activity relationship study. Invest New Drugs. 2009 Dec;27(6):534–42. doi: 10.1007/s10637-008-9205-5.
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