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1-{[(3R,5R)-3-butyl-3-ethyl-7-(methyloxy)-1,1-dioxo-5-phenyl-2,3,4,5-tetrahydro-1,4-benzothiazepin-8-yl]methyl}-L-proline ammonium salt

Base Information
  • Chemical Name:1-{[(3R,5R)-3-butyl-3-ethyl-7-(methyloxy)-1,1-dioxo-5-phenyl-2,3,4,5-tetrahydro-1,4-benzothiazepin-8-yl]methyl}-L-proline ammonium salt
  • CAS No.:1345983-23-4
  • Molecular Formula:C28H38N2O5S*H3N
  • Molecular Weight:531.717
  • Hs Code.:
1-{[(3R,5R)-3-butyl-3-ethyl-7-(methyloxy)-1,1-dioxo-5-phenyl-2,3,4,5-tetrahydro-1,4-benzothiazepin-8-yl]methyl}-L-proline ammonium salt

Synonyms:1-{[(3R,5R)-3-butyl-3-ethyl-7-(methyloxy)-1,1-dioxo-5-phenyl-2,3,4,5-tetrahydro-1,4-benzothiazepin-8-yl]methyl}-L-proline ammonium salt

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Chemical Property of 1-{[(3R,5R)-3-butyl-3-ethyl-7-(methyloxy)-1,1-dioxo-5-phenyl-2,3,4,5-tetrahydro-1,4-benzothiazepin-8-yl]methyl}-L-proline ammonium salt
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Technology Process of 1-{[(3R,5R)-3-butyl-3-ethyl-7-(methyloxy)-1,1-dioxo-5-phenyl-2,3,4,5-tetrahydro-1,4-benzothiazepin-8-yl]methyl}-L-proline ammonium salt

There total 7 articles about 1-{[(3R,5R)-3-butyl-3-ethyl-7-(methyloxy)-1,1-dioxo-5-phenyl-2,3,4,5-tetrahydro-1,4-benzothiazepin-8-yl]methyl}-L-proline ammonium salt 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:
(3R,5R)-3-butyl-3-ethyl-7-(methyloxy)-5-phenyl-2,3,4,5-tetrahydro-1,4-benzothiazepine-8-carbaldehyde 1,1-dioxide; D-proline tert-butyl ester hydrochloride; In dichloromethane; for 1h;
With sodium tris(acetoxy)borohydride; In dichloromethane; at 20 ℃; for 16h;
Guidance literature:
Multi-step reaction with 5 steps
1.1: hydrogenchloride; aluminum (III) chloride / 1,2-dichloro-ethane / 2.5 h / 20 °C
1.2: Cooling with ice
2.1: pyridine / dichloromethane / 0.5 h / 0 - 10 °C / Inert atmosphere
3.1: zinc / 1,1'-bis-(diphenylphosphino)ferrocene; tris-(dibenzylideneacetone)dipalladium(0) / N,N-dimethyl-formamide / 8.25 h / 20 - 80 °C / Inert atmosphere
4.1: diisobutylaluminium hydride / dichloromethane; toluene / 1 h / 0 °C
4.2: 1 h / Cooling with ice
5.1: dichloromethane / 1 h
5.2: 16 h / 20 °C
With pyridine; hydrogenchloride; aluminum (III) chloride; diisobutylaluminium hydride; zinc; 1,1'-bis-(diphenylphosphino)ferrocene; tris-(dibenzylideneacetone)dipalladium(0); In dichloromethane; 1,2-dichloro-ethane; N,N-dimethyl-formamide; toluene;
Guidance literature:
Multi-step reaction with 4 steps
1.1: pyridine / dichloromethane / 0.5 h / 0 - 10 °C / Inert atmosphere
2.1: zinc / 1,1'-bis-(diphenylphosphino)ferrocene; tris-(dibenzylideneacetone)dipalladium(0) / N,N-dimethyl-formamide / 8.25 h / 20 - 80 °C / Inert atmosphere
3.1: diisobutylaluminium hydride / dichloromethane; toluene / 1 h / 0 °C
3.2: 1 h / Cooling with ice
4.1: dichloromethane / 1 h
4.2: 16 h / 20 °C
With pyridine; diisobutylaluminium hydride; zinc; 1,1'-bis-(diphenylphosphino)ferrocene; tris-(dibenzylideneacetone)dipalladium(0); In dichloromethane; N,N-dimethyl-formamide; toluene;
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