ethyl 2-ethoxy-4-<2-<<1-<2-(1-piperidinyl)phenyl>propyl>amino>-2-oxoethyl>-benzoate

Base Information

Chemical Name:ethyl 2-ethoxy-4-<2-<<1-<2-(1-piperidinyl)phenyl>propyl>amino>-2-oxoethyl>-benzoate
CAS No.:1026614-00-5
Molecular Formula:C₂₇H₃₆N₂O₄
Molecular Weight:452.594
Hs Code.:

Synonyms:ethyl 2-ethoxy-4-<2-<<1-<2-(1-piperidinyl)phenyl>propyl>amino>-2-oxoethyl>-benzoate

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Chemical Property of ethyl 2-ethoxy-4-<2-<<1-<2-(1-piperidinyl)phenyl>propyl>amino>-2-oxoethyl>-benzoate

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Technology Process of ethyl 2-ethoxy-4-<2-<<1-<2-(1-piperidinyl)phenyl>propyl>amino>-2-oxoethyl>-benzoate

There total 12 articles about ethyl 2-ethoxy-4-<2-<<1-<2-(1-piperidinyl)phenyl>propyl>amino>-2-oxoethyl>-benzoate 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:

Reference yield: 74.0%

: 219922-19-7
ethyl 2-ethoxy-4-<2-<<1-<5-chloro-2-(1-piperidinyl)phenyl>propyl>amino>-2-oxoethyl>-benzoate

: 1026614-00-5
ethyl 2-ethoxy-4-<2-<<1-<2-(1-piperidinyl)phenyl>propyl>amino>-2-oxoethyl>-benzoate

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; at 50 ℃; for 3h; under 750.06 Torr;
DOI:10.1021/jm9810349

Reference yield:

: 50-85-1
2-hydroxy-p-toluic acid

: 1026614-00-5
ethyl 2-ethoxy-4-<2-<<1-<2-(1-piperidinyl)phenyl>propyl>amino>-2-oxoethyl>-benzoate

Guidance literature:: Multi-step reaction with 7 steps

1: K₂CO₃ / diethyl ether / 30 h / 150 °C

2: N-bromosuccinimide, 2,2'-azo-bis-(isobutyronitril) / CCl₄

3: 97 percent / aq. N-benzyl-tri-n-butylammonium-chloride / CH₂Cl₂ / 43 h / 20 °C

4: HCl / Heating

5: 59 percent / NaOH / ethanol / 1.5 h / 23 - 25 °C

6: 51 percent / PPh₃, Et₃N, CCl₄ / acetonitrile / 15 h / Ambient temperature

7: 74 percent / H₂ / 10 percent Pd/C / ethanol / 3 h / 50 °C / 750.06 Torr

With hydrogenchloride; tetrachloromethane; sodium hydroxide; N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); hydrogen; benzyltri(n-butyl)ammonium chloride; potassium carbonate; triethylamine; triphenylphosphine; palladium on activated charcoal; In tetrachloromethane; diethyl ether; ethanol; dichloromethane; acetonitrile;
DOI:10.1021/jm9810349

Reference yield:

: 88709-17-5
ethyl 2-ethoxy-4-methyl-benzoate

: 1026614-00-5
ethyl 2-ethoxy-4-<2-<<1-<2-(1-piperidinyl)phenyl>propyl>amino>-2-oxoethyl>-benzoate

Guidance literature:: Multi-step reaction with 6 steps

1: N-bromosuccinimide, 2,2'-azo-bis-(isobutyronitril) / CCl₄

2: 97 percent / aq. N-benzyl-tri-n-butylammonium-chloride / CH₂Cl₂ / 43 h / 20 °C

3: HCl / Heating

4: 59 percent / NaOH / ethanol / 1.5 h / 23 - 25 °C

5: 51 percent / PPh₃, Et₃N, CCl₄ / acetonitrile / 15 h / Ambient temperature

6: 74 percent / H₂ / 10 percent Pd/C / ethanol / 3 h / 50 °C / 750.06 Torr

With hydrogenchloride; tetrachloromethane; sodium hydroxide; N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); hydrogen; benzyltri(n-butyl)ammonium chloride; triethylamine; triphenylphosphine; palladium on activated charcoal; In tetrachloromethane; ethanol; dichloromethane; acetonitrile;
DOI:10.1021/jm9810349