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ethyl 5(R)-(E)-7-[2-cyclopropyl-4-(4-fluorophenyl)-quinolin-3-yl]-5-hydroxy-3-oxo-6-heptenoate

Base Information
  • Chemical Name:ethyl 5(R)-(E)-7-[2-cyclopropyl-4-(4-fluorophenyl)-quinolin-3-yl]-5-hydroxy-3-oxo-6-heptenoate
  • CAS No.:254452-95-4
  • Molecular Formula:C27H26FNO4
  • Molecular Weight:447.506
  • Hs Code.:
ethyl 5(R)-(E)-7-[2-cyclopropyl-4-(4-fluorophenyl)-quinolin-3-yl]-5-hydroxy-3-oxo-6-heptenoate

Synonyms:

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Chemical Property of ethyl 5(R)-(E)-7-[2-cyclopropyl-4-(4-fluorophenyl)-quinolin-3-yl]-5-hydroxy-3-oxo-6-heptenoate
Chemical Property:
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SDS file from LookChem

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Technology Process of ethyl 5(R)-(E)-7-[2-cyclopropyl-4-(4-fluorophenyl)-quinolin-3-yl]-5-hydroxy-3-oxo-6-heptenoate

There total 8 articles about ethyl 5(R)-(E)-7-[2-cyclopropyl-4-(4-fluorophenyl)-quinolin-3-yl]-5-hydroxy-3-oxo-6-heptenoate 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:
4-methyleneoxetan-2-one; titanium (IV) ethoxide; (E)-3-[2-cyclopropyl-4-(4-fluoro-phenyl)-quinolin-3-yl]-propenal; With titanium(IV) isopropylate; (S)-2-(N-3-tert-butylsalicylidene)amino-3-methyl-1-butanol; In dichloromethane; at -50 ℃; for 62h;
With oxalic acid; In dichloromethane; at 20 ℃; for 2h; Title compound not separated from byproducts;
DOI:10.1560/PX53-Y9JJ-FU8V-GKEN
Guidance literature:
Multi-step reaction with 6 steps
1: DMSO; P2O5; Et3N
2: NaOH; (n-octyl)3MeNCl / toluene; H2O
3: DIBAH
4: LDA; MgBr2
6: LDA
With sodium hydroxide; phosphorus pentoxide; Aliquat 336; diisobutylaluminium hydride; dimethyl sulfoxide; triethylamine; magnesium bromide; lithium diisopropyl amide; In water; toluene; 1: Oxidation / 2: Condensation / 3: Reduction / 4: Addition / 5: Methylation / 6: Claisen condensation;
DOI:10.1016/S0960-894X(99)00519-3
Guidance literature:
Multi-step reaction with 3 steps
1: LDA; MgBr2
3: LDA
With magnesium bromide; lithium diisopropyl amide; 1: Addition / 2: Methylation / 3: Claisen condensation;
DOI:10.1016/S0960-894X(99)00519-3
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