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(32s,34s,6E,11E,14E,19E)-31,33-di-tert-butyl-8,10,16,18-tetramethyl-9,17-diphenyl-2,4-dioxa-7,8,10,11,15,16,18,19-octaaza-9,17-diphospha-13(2,6)-pyridina-3(2,4)-diazadiphosphetidina-1,5(1,4)-dibenzenacycloicosaphane-6,11,14,19-tetraene 9,17-dioxide | 137918-55-9

分子结构分类

中文名称
——
中文别名
——
英文名称
(32s,34s,6E,11E,14E,19E)-31,33-di-tert-butyl-8,10,16,18-tetramethyl-9,17-diphenyl-2,4-dioxa-7,8,10,11,15,16,18,19-octaaza-9,17-diphospha-13(2,6)-pyridina-3(2,4)-diazadiphosphetidina-1,5(1,4)-dibenzenacycloicosaphane-6,11,14,19-tetraene 9,17-dioxide
英文别名
——
(32s,34s,6E,11E,14E,19E)-31,33-di-tert-butyl-8,10,16,18-tetramethyl-9,17-diphenyl-2,4-dioxa-7,8,10,11,15,16,18,19-octaaza-9,17-diphospha-13(2,6)-pyridina-3(2,4)-diazadiphosphetidina-1,5(1,4)-dibenzenacycloicosaphane-6,11,14,19-tetraene 9,17-dioxide化学式
CAS
137918-55-9
化学式
C45H55N11O4P4
mdl
——
分子量
937.898
InChiKey
JLMFYXUHFCLHCC-LVLAIETCSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    10.02
  • 重原子数:
    64.0
  • 可旋转键数:
    2.0
  • 环数:
    10.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    134.37
  • 氢给体数:
    0.0
  • 氢受体数:
    11.0

反应信息

  • 作为产物:
    参考文献:
    名称:
    Design of new tools for macrocyclic synthesis. Applications to the preparation of polyphosphorus macrocycles
    摘要:
    New diphosphorus m,m' or p,p' dialdehydes 2-7 were prepared by treatment of 1,3-di-tert-butyldiaza-2,4-dichlorodiphosphetidine, 1, with 3- or 4-hydroxybenzaldehyde, and in the case of 4-7 in the presence of S8. These initial compounds when reacted with phosphodihydrazides RP(X) (NCH3NH2)2 9 and 10 allowed the preparation, via [2 + 2] cyclocondensation reactions, of macrocycles 11-13, 15, and 16 possessing six phosphorus atoms in the skeleton, different coordination modes (tri- or tetracoordinate) and both N-P-N and O-P-N linkages. Reaction of the tetraphosphorus dihydrazide 20 with 1,2-benzenedicarboxaldehyde gave macrocycle 22 with a total annular size of 29 ring atoms. Macrocycles 23 or 24 were obtained by reacting 20 with 2,6-pyridinedicarboxaldehyde or 1,3-benzenedicarboxaldehyde. Asymmetry can also be introduced via [1 + 1] cyclocondensation of tetraphosphorus dihydrazides 18 or 19 with diphosphorus dialdehydes 3 or 2; these reactions led to the 38-membered cyclic product 25. Two macrocycles 27, 28 incorporating five phosphorus atoms with three different types of phosphorus environments (C-P-C,N-P-N, and O-P-N) were obtained when tetraphosphorus dihydrazides 18 or 20 were reacted with the phosphorus dialdehyde 26. All the reactions were found stereospecific.
    DOI:
    10.1021/jo00029a034
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同类化合物

()-2-(5-甲基-2-氧代苯并呋喃-3(2)-亚乙基)乙酸乙酯 (甲基3-(二甲基氨基)-2-苯基-2H-azirene-2-羧酸乙酯) (反式)-4-壬烯醛 (双(2,2,2-三氯乙基)) (乙腈)二氯镍(II) (乙基N-(1H-吲唑-3-基羰基)ethanehydrazonoate) (βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (±)17,18-二HETE (±)-辛酰肉碱氯化物 (±)-盐酸氯吡格雷 (±)-丙酰肉碱氯化物 (s)-2,3-二羟基丙酸甲酯 (d(CH2)51,Tyr(Me)2,Arg8)-血管加压素 ([2-(萘-2-基)-4-氧代-4H-色烯-8-基]乙酸) ([1-(甲氧基甲基)-1H-1,2,4-三唑-5-基](苯基)甲酮) (Z)-5-辛烯甲酯 (Z)-4-辛烯醛 (Z)-4-辛烯酸 (Z)-3-[[[2,4-二甲基-3-(乙氧羰基)吡咯-5-基]亚甲基]吲哚-2--2- (S,S)-邻甲苯基-DIPAMP (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-(-)-5'-苄氧基苯基卡维地洛 (S)-(-)-2-(α-(叔丁基)甲胺)-1H-苯并咪唑 (S)-(-)-2-(α-甲基甲胺)-1H-苯并咪唑 (S)-(+)-α-氨基-4-羧基-2-甲基苯乙酸 (S)-(+)-5,5'',6,6'',7,7'',8,8''-八氢-3,3''-二叔丁基-1,1''-二-2-萘酚,双钾盐 (S)-阿拉考特盐酸盐 (S)-赖诺普利-d5钠 (S)-盐酸沙丁胺醇 (S)-溴烯醇内酯 (S)-氨氯地平-d4 (S)-氨基甲酸酯β-D-O-葡糖醛酸 (S)-8-氟苯并二氢吡喃-4-胺 (S)-7,7-双[(4S)-(苯基)恶唑-2-基)]-2,2,3,3-四氢-1,1-螺双茚满 (S)-4-(叔丁基)-2-(喹啉-2-基)-4,5-二氢噁唑 (S)-4-氯-1,2-环氧丁烷 (S)-3-(((2,2-二氟-1-羟基-7-(甲基磺酰基)-2,3-二氢-1H-茚满-4-基)氧基)-5-氟苄腈 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-3-(2-(二氟甲基)吡啶-4-基)-7-氟-3-(3-(嘧啶-5-基)苯基)-3H-异吲哚-1-胺 (S)-2-(环丁基氨基)-N-(3-(3,4-二氢异喹啉-2(1H)-基)-2-羟丙基)异烟酰胺 (S)-2-氨基-5-氧代己酸,氢溴酸盐 (S)-2-[[[(1R,2R)-2-[[[3,5-双(叔丁基)-2-羟基苯基]亚甲基]氨基]环己基]硫脲基]-N-苄基-N,3,3-三甲基丁酰胺 (S)-2-[3-[(1R,2R)-2-(二丙基氨基)环己基]硫脲基]-N-异丙基-3,3-二甲基丁酰胺 (S)-2-N-Fmoc-氨基甲基吡咯烷盐酸盐 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-(4-氨基氧基乙酰胺基苄基)乙二胺四乙酸 (S)-1-[N-[3-苯基-1-[(苯基甲氧基)羰基]丙基]-L-丙氨酰基]-L-脯氨酸 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (SP-4-1)-二氯双(喹啉)-钯 (SP-4-1)-二氯双(1-苯基-1H-咪唑-κN3)-钯