CAS: 21685-47-2; O-Methyl-D-Valine

该化合物是一种受保护的醋酸衍生物,一种基本氨基酸,其蛋白质组是甲基的,氨基类是无盐的盐,该化合物作为一种构件被广泛用作浸泡物合成的构件,其优点包括有机溶剂的溶性得到改善,以及混合反应过程中的稳定性增强.盐化物形式确保了更好的处理和储存,而甲基酯保护则有利于在温和条件下有选择地减少保护.其高纯度和持续的质量使它适合药物研究,特别是在生物活性聚苯醚和聚苯乙烯合成过程中的开发.该产品的特点是在固相和溶性合成阶段的可靠性能.

结构式图片

相似化合物

7146-15-8 154674-67-6 4070-48-8

上下游产品

methanol D-Val-OH tert-butyl dicarbonatedi-tert-butyl dicarbonate (3S,6R)-6-Isopropyl-5,8-dimethoxy-1-phenyl-4,7-diaza-spiro[2.5]°Cta-1,4,7-trieneN-[(Ξ)-1-methoxycarbonyl-1-(2-phenyl-acetylamino)-ethyl]-D-valine methyl esterN-[(Ξ)-1-methoxycarbonyl-1-(2-phenyl-acetylamino)-ethyl]-D-valine methyl ester N-[(S)-2-methoxycarbonyl-2-(2-phenyl-acetylamino)-ethyl]-D-valine methyl esterN-[(S)-2-methoxycarbonyl-2-(2-phenyl-acetylamino)-ethyl]-D-valine methyl ester N-[(R)-2-methoxycarbonyl-2-(2-phenyl-acetylamino)-ethyl]-D-valine methyl esterN-[(R)-2-methoxycarbonyl-2-(2-phenyl-acetylamino)-ethyl]-D-valine methyl ester Z-Ala-D-Val-OMe

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    专利信息


    专利号:US-8653282-B2
    优先权日:2007-10-18
    标 题:Preparation of dihydrothieno [3,2-D] pyrimidines and intermediates used therein
    发明人:FRUTOS ROGELIO; KRISHNAMURTHY DHILEEPKUMAR; MULDER JASON ALAN; RODRIGUEZ SONIA; SENANAYAKE CHRIS HUGH; TAMPONE THOMAS G
    权利人:FRUTOS ROGELIO; KRISHNAMURTHY DHILEEPKUMAR; MULDER JASON ALAN; RODRIGUEZ SONIA; SENANAYAKE CHRIS HUGH; TAMPONE THOMAS G; BOEHRINGER INGELHEIM INT
    摘要:The invention relates to improved methods of preparing dihydrothienopyrimidines of formula 1, and intermediates thereof, (I) wherein X is SO or SO 2 , preferably SO, and wherein R A , R 1 , R 2 , R 3 , R 4 and R 5 have the meanings given in the description. The methods according to this invention are more suitable for large-scale synthesis of said compounds than prior methods because the new synthetic process avoids distillation and chromatographic purification between steps and results in a higher overall yield of the desired product.

    专利号:US-9422321-B2
    优先权日:2010-09-07
    标题 :Pyrimidine nucleoside derivatives, synthesis methods and uses thereof for preparing anti-tumor and anti-virus medicaments
    发明人:CHANG JUNBIAO; AN HAOYUN; YU XUEJUN; GUO XIAOHE
    权利人:CHANG JUNBIAO; AN HAOYUN; YU XUEJUN; GUO XIAOHE; HIGH & NEW TECH RES CENTER HENAN ACAD OF SCIENCES; ZHENGZHOU GRANLEN PHARMATECH LTD; UNIV ZHENGZHOU
    摘要:The present invention relates to the field of pharmacochemistry. Disclosed are fluorinated and azido-substituted pyrimidine nucleoside derivatives, particularly compounds of the formula shown below: n nAlso disclosed are methods of preparation and uses for these compounds. The compounds can be used for preparing medicaments for treating diseases such as tumors and viral infections, and can be used separately or in combination with other medicaments. The compounds also have effective activity against diseases such as tumors and viral infections, while having few side effects, and thus have potential application value.

    专利号:US-10233182-B2
    优先权日:2014-04-04
    标题 :Substituted spirocyclic inhibitors of autotaxin
    发明人:BABISS LEE; CLARK MATTHEW; KEEFE ANTHONY D; MULVIHILL MARK J; NI HAIHONG; RENZETTI LOUIS; RUEBSAM FRANK; WANG CE; XIE ZHIFENG; ZHANG YING
    权利人:X RX INC
    摘要:The present invention relates to compounds according to Formula I and pharmaceutically acceptable salts, synthesis, intermediates, formulations, and methods of disease treatment therewith, including cancer, lymphocyte homing, chronic inflammation, neuropathic pain, fibrotic diseases, thrombosis, and cholestatic pruritus, mediated at least in part by ATX.

    专利号:US-2002077491-A1
    优先权日:2000-09-05
    标 题 :Methods for forming combinatorial libraries combining amide bond formation with epoxide opening
    发明人:SHIPPS GERALD W; ROSNER KRISTIN E; MAKARA GERGELY M; WINTNER EDWARD A; NASH HUW M; FELSCH JASON S; PAL KOLLOL; LENZ GEORGE R
    摘要:The invention relates to methods for forming combinatorial libraries. The invention provides methods suitable for the rapid and convenient synthesis of very large combinatorial libraries of small organic molecules. In particular, the invention provides a method for forming combinatorial libraries combining amide bond formation with epoxide opening.

    专利号:JP-2011139667-A
    优先权日:2010-01-07
    标题:Dipeptide having proline and β-alanine at the N-terminus, and method for enzymatic synthesis of the cyclized dipeptide

    专利号:CN-108129404-B
    优先权日:2018-01-30
    标题 :Synthesis method of chiral piperazinone derivative
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    摘要:Seidel, D., Science of Synthesis Knowledge Updates, (2012) 3, 427.
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