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(3S)-1-(carboxymethyl)-3-<<(1S)-1-(ethoxycarbonyl)-3-phenylpropyl>amino>-3,4,5,6-tetrahydro-<1>benzazocin-2-(1H)-one hydrochloride

Base Information
  • Chemical Name:(3S)-1-(carboxymethyl)-3-<<(1S)-1-(ethoxycarbonyl)-3-phenylpropyl>amino>-3,4,5,6-tetrahydro-<1>benzazocin-2-(1H)-one hydrochloride
  • CAS No.:97278-76-7
  • Molecular Formula:C25H30N2O5*ClH
  • Molecular Weight:474.985
  • Hs Code.:
(3S)-1-(carboxymethyl)-3-<<(1S)-1-(ethoxycarbonyl)-3-phenylpropyl>amino>-3,4,5,6-tetrahydro-<1>benzazocin-2-(1H)-one hydrochloride

Synonyms:(3S)-1-(carboxymethyl)-3-<<(1S)-1-(ethoxycarbonyl)-3-phenylpropyl>amino>-3,4,5,6-tetrahydro-<1>benzazocin-2-(1H)-one hydrochloride

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Chemical Property of (3S)-1-(carboxymethyl)-3-<<(1S)-1-(ethoxycarbonyl)-3-phenylpropyl>amino>-3,4,5,6-tetrahydro-<1>benzazocin-2-(1H)-one hydrochloride
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Technology Process of (3S)-1-(carboxymethyl)-3-<<(1S)-1-(ethoxycarbonyl)-3-phenylpropyl>amino>-3,4,5,6-tetrahydro-<1>benzazocin-2-(1H)-one hydrochloride

There total 6 articles about (3S)-1-(carboxymethyl)-3-<<(1S)-1-(ethoxycarbonyl)-3-phenylpropyl>amino>-3,4,5,6-tetrahydro-<1>benzazocin-2-(1H)-one hydrochloride 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 6 steps
1: 50 percent / PCl5, Br2, I2 / CHCl3 / 4 h / Heating
2: 83 percent / sodium azide / dimethylsulfoxide / 5 h / 60 °C
3: 57 percent / potassium tert-butoxide / tetrahydrofuran / 36 h / Ambient temperature
4: 9.2 g / di-n-butyltin dichloride / CHCl3 / 24 h / Heating
5: 1.0 g / sodium cyanoborohydride / methanol; acetic acid / 18 h / Ambient temperature
6: 0.6 g / H2 / 10percent Pd/C / ethanol / 760 Torr / Ambient temperature
With sodium azide; phosphorus pentachloride; dibutyltin chloride; potassium tert-butylate; hydrogen; bromine; iodine; sodium cyanoborohydride; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; chloroform; acetic acid; dimethyl sulfoxide;
DOI:10.1021/jm00148a023
Guidance literature:
Multi-step reaction with 5 steps
1: 83 percent / sodium azide / dimethylsulfoxide / 5 h / 60 °C
2: 57 percent / potassium tert-butoxide / tetrahydrofuran / 36 h / Ambient temperature
3: 9.2 g / di-n-butyltin dichloride / CHCl3 / 24 h / Heating
4: 1.0 g / sodium cyanoborohydride / methanol; acetic acid / 18 h / Ambient temperature
5: 0.6 g / H2 / 10percent Pd/C / ethanol / 760 Torr / Ambient temperature
With sodium azide; dibutyltin chloride; potassium tert-butylate; hydrogen; sodium cyanoborohydride; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; chloroform; acetic acid; dimethyl sulfoxide;
DOI:10.1021/jm00148a023
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