CAS: 71904-80-8; 2-(((Tert-Butoxycarbonyl)Amino)Methyl)Thiazole-4-Carboxylic Acid

该化合物是一种化学化合物,其特点是硫化环,即五人组成的含有硫和氮的环环环结构;该化合物是一个碳酸酸功能组,有助于其酸性和在各种化学反应中的潜在反应反应.二丁氧碳基(Boc)组是该矿的防护组,在合成和操纵过程中加强了分子的稳定性.氨基生物组的存在允许进一步衍生,使其在硫化物合成和药用化学中有用.硫酸混合物通常与生物活动有关,包括抗微生物和抗硫特性.该化合物通常用于研究和开发,特别是在有机合成和制药化学领域.其溶性性和稳定性取决于溶剂和条件,而这些是实验室环境中应用该化合物的重要考虑因素.

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ECHA物质C&L通报

上下游产品

bromopyruvic acid 2-(N-t-butoxycarbonylamino)thioacetamide tert-butyl dicarbonatedi-tert-butyl dicarbonate 2-(aminomethyl)thiazole-4-carboxylic acid hydr°Chloride (S)-1-((R)-2-Amino-3,3-diphenyl-propionyl)-pyrrolidine-2-carboxylic acid (4-cyano-thiazol-2-ylmethyl)-amide 2-((S)-1-{[2-((R)-1-{[2-(tert-Butoxycarbonylamino-methyl)-thiazole-4-carbonyl]-amino}-2-methyl-propyl)-thiazole-4-carbonyl]-amino}-ethyl)-5-methyl-oxazole-4-carboxylic acid pentafluorophenyl ester (S)-1-((S)-2-{(S)-2-[(2-{1-[(2-Aminomethyl-thiazole-4-carbonyl)-amino]-3-carbamoyl-propyl}-thiazole-4-carbonyl)-amino]-3-methyl-butyrylamino}-4-methyl-pentanoyl)-pyrrolidine-2-carboxylic acid 2,4,5-trichloro-phenyl ester; compound with trifluoro-acetic acid (S)-1-[(S)-2-((S)-2-{[2-(1-{[2-(tert-Butoxycarbonylamino-methyl)-thiazole-4-carbonyl]-amino}-3-carbamoyl-propyl)-thiazole-4-carbonyl]-amino}-3-methyl-butyrylamino)-4-methyl-pentanoyl]-pyrrolidine-2-carboxylic acid 2,4,5-trichloro-phenyl ester

合成工艺路线路线简述

  • 合成目标产物 2-[[(Tert-Butoxycarbonyl)Amino]Methyl]Thiazole-4-Carboxylic Acid 主要起始原料 Tert-Butyl (4-(Ethoxycarbonyl)Thiazol-2-yl)Methylcarbamate
  • (文献来源)合成步骤主要原料 Tert-Butyl (4-(Ethoxycarbonyl)Thiazol-2-yl)Methylcarbamate
📜Boc-Gly-ocooet置于劳森试剂,2,6-二甲基吡啶,Lithium Hydroxide,Ammonium Hydroxide,Potassium Hydrogencarbonate,三氟乙酸酐体系中,用 四氢呋喃,甲醇,乙二醇二甲醚,二氯甲烷 作为反应溶剂,化学反应 36.25H,反应生成 2-[[(叔丁氧羰基)氨基]甲基]噻唑-4-羧酸
参考文献:Moody,Christopher J.; Bagley,Mark C.,Journal Of The Chemical Society. Perkin Transactions I,1998,# 3,P. 601-607
标题:Moody,Christopher J.; Bagley,Mark C.,Journal Of The Chemical Society. Perkin Transactions I,1998,# 3,P. 601-607

海关参考信息

专利信息


专利号:US-2019031650-A1
优先权日:2016-01-29
标 题 :Dna alkylation and cross-linking agents as compounds and payloads for targeted therapies
发明人:HERZON SETH; HEALY ALAN; CRAWFORD JASON; VIZCAINO MARIA; NIKOLAYEVSKIY HERMAN
权利人:UNIV YALE
摘要:The present invention is directed to compounds related to precolibactin pharmaceutical compositions based upon these compounds and methods of synthesis which are employed to provide intermediates and final compounds, which are principally alkylating agents and anticancer compounds. The chemical synthetic approach disclosed facilitates the synthesis of numerous precolibactin analogs which can be used in the treatment of cancer.

专利号:WO-0127095-A1
优先权日:1999-10-14
标 题:Method for producing 2-(n-boc-aminomethyl)-thiazol-4-carboxylic acid
发明人:BUSCHMANN ERNST; PFEIFFER THOMAS
权利人:BASF AG; BUSCHMANN ERNST; PFEIFFER THOMAS
摘要:The synthesis of dolastatin 3, which inhibits cell growth, requires a 2-aminomethyl-thiazol-4-carboxylic acid that is protected on the amino group as a building block. The invention provides a synthesis for producing this compound with a high degree of purity and a high yield so that it is also feasible on an industrial scale. To this end, a glycine thioamide with a protective group on the amino group is reacted preferably with 3-brom-2-oxo-propionic acid in the presence of at least one tertiary amine.

专利号:US-2010113305-A1
优先权日:1999-03-22
标题:Oxazole and thiazole combinatorial libraries
发明人:MARTIN LENORE M; HU BI-HUANG
权利人:RHODE ISLAND EDUCATION
摘要:This invention provides a novel method for synthesizing an ensemble of peptides that allows for the generation of an unlimited number of antibiotic compounds. More specifically, the method comprises utilizes synthetic heterocyclic amino acids containing thaizole and/or oxazole as building blocks in a solid phase combinatorial synthesis to yield natural and unnatural antibiotic compounds.

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📌 第三方产品分析报告

✅ COA系统入驻 | 共享模式

合成参考文献


参考文献:10.1055/s-0029-1216931
摘要:Forsyth C, Wang B. Total Synthesis of Largazole - Devolution of a Novel Synthetic Strategy. Synthesis. 2009 Aug 14;2009(17):2873–80. doi: 10.1055/s-0029-1216931.
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