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7,16-bis<4-<1-(3,5-dimethoxycarbonyl)phenyl-4,5-dihydro-1H-pyrazol-3-yl>phenyl>-1,4,10,13-tetraoxa-7,16-diazacyclooctadecane

Base Information Edit
  • Chemical Name:7,16-bis<4-<1-(3,5-dimethoxycarbonyl)phenyl-4,5-dihydro-1H-pyrazol-3-yl>phenyl>-1,4,10,13-tetraoxa-7,16-diazacyclooctadecane
  • CAS No.:226936-47-6
  • Molecular Formula:C50H58N6O12
  • Molecular Weight:935.044
  • Hs Code.:
  • Mol file:226936-47-6.mol
7,16-bis<4-<1-(3,5-dimethoxycarbonyl)phenyl-4,5-dihydro-1H-pyrazol-3-yl>phenyl>-1,4,10,13-tetraoxa-7,16-diazacyclooctadecane

Synonyms:7,16-bis<4-<1-(3,5-dimethoxycarbonyl)phenyl-4,5-dihydro-1H-pyrazol-3-yl>phenyl>-1,4,10,13-tetraoxa-7,16-diazacyclooctadecane

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Chemical Property of 7,16-bis<4-<1-(3,5-dimethoxycarbonyl)phenyl-4,5-dihydro-1H-pyrazol-3-yl>phenyl>-1,4,10,13-tetraoxa-7,16-diazacyclooctadecane Edit
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Technology Process of 7,16-bis<4-<1-(3,5-dimethoxycarbonyl)phenyl-4,5-dihydro-1H-pyrazol-3-yl>phenyl>-1,4,10,13-tetraoxa-7,16-diazacyclooctadecane

There total 7 articles about 7,16-bis<4-<1-(3,5-dimethoxycarbonyl)phenyl-4,5-dihydro-1H-pyrazol-3-yl>phenyl>-1,4,10,13-tetraoxa-7,16-diazacyclooctadecane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 4 steps
1: 28 percent / tetrabutylammonium fluoride trihydrate / 12 h / 150 °C
2: 1.) LDA / 1) THF, heptane, -78 deg C, 1 h; 2) THF, heptane, 0 deg C, 2 h
3: 75 percent / NaHCO3, NaIO4 / tetrahydrofuran; methanol; H2O / 0.5 h / Ambient temperature
4: 52 percent / acetic acid / 264 h / Ambient temperature; further reagent and conditions
With sodium periodate; tetrabutyl ammonium fluoride; sodium hydrogencarbonate; lithium diisopropyl amide; In tetrahydrofuran; methanol; water; acetic acid;
DOI:10.1016/S0040-4020(99)00167-2
Guidance literature:
Multi-step reaction with 3 steps
1: 1.) sodium nitrite, aq. HCl, 2.) sodium sulphite, 3.) conc. HCl / 1) water, 0-5 deg C, 1 h; 2) water, 50-60 deg C, 45 min; 3) water, 90 deg C, 1 hi930
2: H2SO4 / 2 h / Heating
3: 52 percent / acetic acid / 264 h / Ambient temperature; further reagent and conditions
With hydrogenchloride; sulfuric acid; sodium sulfite; sodium nitrite; In acetic acid;
DOI:10.1016/S0040-4020(99)00167-2
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