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    • 7. 发明申请
    • Mobile gas turbine engine and generator assembly
    • 移动燃气涡轮发动机和发电机总成
    • US20060254281A1
    • 2006-11-16
    • US11130356
    • 2005-05-16
    • Gilbert BadeerNarendra Joshi
    • Gilbert BadeerNarendra Joshi
    • F02C7/143
    • F02C6/203F02C7/143F02C7/16F05B2240/931F05D2220/76Y02T50/675
    • A method for supplying power to a remote load includes coupling a gas turbine engine to a vessel that is not used to provide propulsion for the vessel, coupling a generator to the gas turbine engine, coupling an intercooler system downstream from a first compressor such that compressed air discharged from the first compressor is channeled therethrough, the intercooler system includes an intercooler and a first heat exchanger, channeling a first working fluid through the intercooler to facilitate reducing an operating temperature of air discharged from the intercooler to a second compressor, channeling a second working fluid flowing through the first heat exchanger to extract energy from the first working fluid to facilitate reducing an operating temperature of the first working fluid, and operating the gas turbine engine and generator to supply power to a load that is located remotely from the vessel.
    • 用于向远程负载供电的方法包括将燃气涡轮发动机联接到不用于为船舶提供推进力的容器,将发电机联接到燃气涡轮发动机,将中间冷却器系统从第一压缩机下游连接到压缩机 从第一压缩机排出的空气被引导通过,中间冷却器系统包括中间冷却器和第一热交换器,将第一工作流体引导通过中间冷却器,以便于将从中间冷却器排出的空气的工作温度降低到第二压缩机, 工作流体流过第一热交换器以从第一工作流体提取能量,以便于降低第一工作流体的工作温度,以及操作燃气涡轮发动机和发电机,以向远离容器的负载供电。
    • 10. 发明授权
    • Process for the preparation of pyrimidine derivatives
    • 制备嘧啶衍生物的方法
    • US07312329B2
    • 2007-12-25
    • US11004755
    • 2004-12-03
    • Narendra JoshiShekhar Bhaskar BhirudBatchu ChandrasekharK. Eswara RaoSubhash Damle
    • Narendra JoshiShekhar Bhaskar BhirudBatchu ChandrasekharK. Eswara RaoSubhash Damle
    • C07F9/02C07D239/02
    • C07D239/42Y02P20/55
    • An improved process for the preparation of pyrimidine derivatives is provided comprising reacting a Wittig reagent of the general formula wherein R is an alkyl of from 1 to 10 carbon atoms, aryl or arylalkyl, R1 is a substituted or unsubstituted hydrocarbon group, R2 and R3 are the same or different and are hydrogen or a substituted or unsubstituted hydrocarbon group; Z is sulfur, oxygen, sulfonyl, or imino which may be substituted by formyl, acetyl, propionyl, butyryl, isobutyryl, valeryl, isovaleryl, amino substituted by sulfonyl or alkylsulfonyl, and sulfonyl substituted by alkyl, amino or alkylamino and X is a halogen; with an aldehyde of the general formula wherein R4 is hydrogen, a lower alkyl or a cation capable of forming a non-toxic pharmaceutically acceptable salt and each R5 are the same or different and are hydrogen or a hydrolyzable protecting group, or each R5, together with the oxygen atom to which each is bonded, form a hydrolyzable cyclic protecting group, or each R5 is bonded to the same substituent which is bonded to each oxygen atom to form a hydrolyzable protecting group; in the presence of a base.
    • 提供了制备嘧啶衍生物的改进方法,包括使通式为Wittig试剂反应其中R为1至10个碳原子的烷基,芳基或芳基烷基,R 1是被取代或 未取代的烃基,R 2和R 3相同或不同,为氢或取代或未取代的烃基; Z可以被甲酰基,乙酰基,丙酰基,丁酰基,异丁酰基,戊酰基,异戊酰基,被磺酰基或烷基磺酰基取代的氨基,和被烷基,氨基或烷基氨基取代的磺酰基取代的硫,氧,磺酰基或亚氨基,X是卤素 ; 与其中R 4为氢的通式的醛,能够形成无毒的药学上可接受的盐的低级烷基或阳离子和每个R 5相同 或不同的是氢或可水解保护基团,或每个R 5与每个键合的氧原子一起形成可水解的环保护基团,或每个R 5, SUP>键合到与每个氧原子键合的相同取代基以形成可水解保护基团; 在一个基地的存在。