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3-{4-[3-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-thiadiazol-3-yl)-2-ethylphenyl]-1-piperidinyl}propanoic acid

Base Information
  • Chemical Name:3-{4-[3-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-thiadiazol-3-yl)-2-ethylphenyl]-1-piperidinyl}propanoic acid
  • CAS No.:1344997-19-8
  • Molecular Formula:C27H32ClN3O3S
  • Molecular Weight:514.088
  • Hs Code.:
3-{4-[3-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-thiadiazol-3-yl)-2-ethylphenyl]-1-piperidinyl}propanoic acid

Synonyms:3-{4-[3-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-thiadiazol-3-yl)-2-ethylphenyl]-1-piperidinyl}propanoic acid

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Chemical Property of 3-{4-[3-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-thiadiazol-3-yl)-2-ethylphenyl]-1-piperidinyl}propanoic acid
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Technology Process of 3-{4-[3-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-thiadiazol-3-yl)-2-ethylphenyl]-1-piperidinyl}propanoic acid

There total 11 articles about 3-{4-[3-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-thiadiazol-3-yl)-2-ethylphenyl]-1-piperidinyl}propanoic acid 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:
3-bromo-5-(3-chloro-4-isopropoxyphenyl)-1,2,4-thiadiazole; ethyl 3-{4-[2-ethyl-3-(4,4,5-trimethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1-piperidinyl}propanoate; With potassium phosphate; tetrakis(triphenylphosphine) palladium(0); at 120 ℃; for 0.333333h; Biotage Initiator; Sealed; Inert atmosphere;
With water; sodium hydroxide; In isopropyl alcohol; at 50 ℃; for 2h;
With acetic acid; In isopropyl alcohol;
Guidance literature:
C29H36ClN3O3S; With water; sodium hydroxide; In isopropyl alcohol; at 50 ℃; for 2h;
With acetic acid; In water; isopropyl alcohol;
Guidance literature:
Multi-step reaction with 7 steps
1: n-butyllithium / hexane; tetrahydrofuran / 4 h / -78 °C / Inert atmosphere
2: hydrogenchloride; acetic acid / water / 12 h / Reflux
3: potassium acetate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2 / 1,4-dioxane / 90 °C / Inert atmosphere
4: hydrogen / palladium 10% on activated carbon / ethyl acetate / 12 h / 50 °C / 2844.39 Torr
5: 1,8-diazabicyclo[5.4.0]undec-7-ene / acetonitrile / 2 h / 80 °C / Sealed vessel
6: potassium phosphate / tetrakis(triphenylphosphine) palladium(0) / N,N-dimethyl-formamide; water / 0.33 h / 120 °C / Sealed vessel; Inert atmosphere; Microwave irradiation
7: sodium hydroxide; water / isopropyl alcohol / 2 h / 50 °C
With hydrogenchloride; potassium phosphate; n-butyllithium; water; hydrogen; potassium acetate; acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; sodium hydroxide; tetrakis(triphenylphosphine) palladium(0); dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; palladium 10% on activated carbon; In tetrahydrofuran; 1,4-dioxane; hexane; water; ethyl acetate; N,N-dimethyl-formamide; isopropyl alcohol; acetonitrile; 6: Suzuki Coupling;
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