CAS: 14220-64-5; Bis(Benzonitrile)Palladium Chloride

上下游产品

benzonitrile 2(P(C6H5)(2-C6H4Cl)2)2PdCl2(P(C6H5)(2-C6H4Cl)2)2 hydrogenchloride palladium diacetatedichloro([2-(3-pyrazolyl)phenyl]diphenylphosphine) palladium(II) [Pd(η3-phenethyl)((R)-BINAP)](triflate) [Pd(η3-naphthylethyl)((R)-BINAP)](triflate) (bis(diphenylphosphino)methane)palladium(II) dichloride

Palladium(II) Chloride,苯甲腈 以 苯甲腈 用作溶剂,化学反应生成二(氰基苯)二氯化钯
参考文献:钯(II)配合物与烯烃配体的热分解研究
标题:钯(II)配合物与烯烃配体的热分解研究
摘要:摘要 Pdcl2(Vtms)2 (1),Pdcl2(Ptmsa)2 (2),Pdcl2(Dmb)2 (3) 和 Pdcl2(Dadms)2 (4),其中 Vtms-三甲基(乙烯基)硅烷,Dadms-二烯丙基二甲基硅烷,制备了 Ptmsa-1-苯基-2-(三甲基甲硅烷基)乙炔和 Dmb-2,3-二甲基-2-丁烯,并通过 Tg/dtg/dta 技术研究了热特性.Tg/ir 方法用于 303-573 K 范围内配体和配合物的气相研究.Ms-Ei 分析数据用于阐明气相中的金属化物质.热分析结果表明有机配体在分解的第一阶段脱离,而氯分子在第二阶段脱离.金属钯是分解的最终产物,通过对加热至 1273 K 的残留物进行 Xrd 分析证实了这一点.金属钯是在 478-720 K 的温度范围内形成的,是什么使配合物 (1-4) 成为有前途的化学气相沉积 (Cvd) 前体.所有钯 (II) 配合物的 Tg/ir
Doi:10.1016/j.Tca.2009.06.002

专利信息

专利号:US-8822702-B2
优先权日:2002-12-20
标 题 :Synthesis of amines and intermediates for the synthesis thereof
发明人：BERENS ULRICH; DOSENBACH OLIVER; SPRENGER DANIEL
权利人:BERENS ULRICH; DOSENBACH OLIVER; SPRENGER DANIEL; BASF SE
摘要:The invention relates in a first embodiment to a method for the manufacture of esters of the formula I, n nor especially of amides of the formula II,n n nwherein the symbols have the meanings given in the specification, as well as other intermediates and compounds useful in the synthesis of tryptamines and other substances mentioned in the title. The synthesis methods and intermediates are useful in the synthesis of pharmaceuticals.

专利号:WO-2025119975-A1
优先权日:2023-12-04
标 题:A method for synthesis of harmine
发明人：HETT ROBERT; GRAB HANUSCH; LAGOUTTE ROMAN
权利人:RECONNECT LABS AG
摘要:The invention relates to a method of synthesis of a compound of formula (I), harmine, according to the method comprising a step of transforming the compound of formula (II), into the compound of formula (I). The invention further relates to a compound of formula (II), which is an intermediate in synthesis of harmine according to the present invention.

专利号:EP-0842924-B1
优先权日:1996-11-14
标 题 :Pyridine intermediates, useful in the synthesis of beta-adrenergic receptor agonists
发明人：WRIGHT STEPHEN WAYNE
权利人:PFIZER
摘要:The present invention relates to certain compounds of the formula (I), which are useful in the synthesis of certain beta -adrenergic receptor agonists. The invention also relates to a process for synthesizing the compounds of formula (I) and to compounds of the formula (II), wherein R<1>, R<2> and R<4> are defined herein, which are useful in the synthesis of the compounds of formula (I). The invention also relates to a process for synthesizing a compound of formula (II). The invention further relates to processes for synthesizing compounds of formula (Z*), R<1>, R<2> and Y<2*> are defined herein.o

专利号:US-2007249867-A1
优先权日:2004-08-11
标题 :Method for Synthesis of Aromatic Amine
发明人：NAKASHIMA HARUE; KAWAKAMI SACHIKO
权利人:NAKASHIMA HARUE; KAWAKAMI SACHIKO
摘要:One embodiment of the present invention provides a method for synthesis of substituted secondary amine by the reaction of aniline with aryl halide by using a Pd catalyst including (t-Bu) 3 P as a ligand.

专利号:WO-2024073221-A1
优先权日:2022-09-29
标题:Synthesis of palladium(0) phosphine complexes
发明人：MACQUEEN PRESTON; GHORAI SUBIR; COLACOT THOMAS
权利人:SIGMA ALDRICH CO LLC
摘要:Provided is an optimized process for the synthesis of palladium(O) phosphine complexes. The process described herein is characterized by a more efficient reaction control, high yield and purity, the use of readily available starting materials, and savings in reaction time and steps, thereby offering increased sustainability when compared to processes reported in the state of the art.

专利号:US-2025101006-A1
优先权日:2022-01-31
标题:Process for the synthesis of pyrazolyl derivatives useful as anti-cancer agents
发明人：BAENZIGER MARKUS; GALLOU FABRICE; GUO FENGFENG; HÄNGGI RUDOLF; HAN ENJIAN; JORDINE GUIDO; LI JIALIANG; LIU WEIPENG; MIAO BUKEYAN; RONG SHAOFENG; SANTANDREA ERNESTO; SCHIRNER PAUL BERND; SHEN XIAODONG; WANG CAN; ZHANG HAO
权利人:NOVARTIS AG
摘要:The invention provides a novel process, novel process steps and novel intermediates useful in the synthesis of pharmaceutically active compounds, especially KRAS G12C inhibitors. The present invention provides a direct enantioselective chemical manufacturing method of making Compound A, or a pharmaceutically acceptable hydrate or solvent thereof: (I). The invention provides a process for preparing Intermediate B6* comprising reacting Intermediate B4* with Intermediate B5* in an atroposelective coupling reaction, using a chiral catalyst.