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Phosphoric acid (2R,3R,4R,5R)-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(2-methoxy-ethoxymethoxy)-5-[3-(2-methoxy-ethoxymethyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-tetrahydro-furan-3-yl ester 5-chloro-quinolin-8-yl ester; compound with triethyl-amine

Base Information Edit
  • Chemical Name:Phosphoric acid (2R,3R,4R,5R)-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(2-methoxy-ethoxymethoxy)-5-[3-(2-methoxy-ethoxymethyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-tetrahydro-furan-3-yl ester 5-chloro-quinolin-8-yl ester; compound with triethyl-amine
  • CAS No.:100190-49-6
  • Molecular Formula:C6H15N*C47H51ClN3O15P
  • Molecular Weight:1065.55
  • Hs Code.:
  • Mol file:100190-49-6.mol
Phosphoric acid (2R,3R,4R,5R)-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(2-methoxy-ethoxymethoxy)-5-[3-(2-methoxy-ethoxymethyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-tetrahydro-furan-3-yl ester 5-chloro-quinolin-8-yl ester; compound with triethyl-amine

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Chemical Property of Phosphoric acid (2R,3R,4R,5R)-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(2-methoxy-ethoxymethoxy)-5-[3-(2-methoxy-ethoxymethyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-tetrahydro-furan-3-yl ester 5-chloro-quinolin-8-yl ester; compound with triethyl-amine Edit
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Technology Process of Phosphoric acid (2R,3R,4R,5R)-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(2-methoxy-ethoxymethoxy)-5-[3-(2-methoxy-ethoxymethyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-tetrahydro-furan-3-yl ester 5-chloro-quinolin-8-yl ester; compound with triethyl-amine

There total 5 articles about Phosphoric acid (2R,3R,4R,5R)-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(2-methoxy-ethoxymethoxy)-5-[3-(2-methoxy-ethoxymethyl)-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]-tetrahydro-furan-3-yl ester 5-chloro-quinolin-8-yl ester; compound with triethyl-amine 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: tetrahydrofuran / 16 h / Heating
2: 1 M tributylammonium fluoride (TBAHF) / tetrahydrofuran / 3 h / Ambient temperature
3: 95 percent / pyridine / 1 h
4: 88 percent / 8-quinolinesulfonyl chloride (QS-Cl), pyridine / 2 h / Ambient temperature
With pyridine; quinoline-8-sulfonyl chloride; tri-n-butylamine hydrofluoride; In tetrahydrofuran;
DOI:10.1021/jo00356a033
Guidance literature:
Multi-step reaction with 3 steps
1: 1 M tributylammonium fluoride (TBAHF) / tetrahydrofuran / 3 h / Ambient temperature
2: 95 percent / pyridine / 1 h
3: 88 percent / 8-quinolinesulfonyl chloride (QS-Cl), pyridine / 2 h / Ambient temperature
With pyridine; quinoline-8-sulfonyl chloride; tri-n-butylamine hydrofluoride; In tetrahydrofuran;
DOI:10.1021/jo00356a033
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