3-[(1S)-2-[(3S)-3-[(tert-butyldimethylsilyl)oxy]pyrrolidin-1-yl]-1-(methylamino)ethyl]benzoic acid

Base Information

Chemical Name:3-[(1S)-2-[(3S)-3-[(tert-butyldimethylsilyl)oxy]pyrrolidin-1-yl]-1-(methylamino)ethyl]benzoic acid
CAS No.:1455472-91-9
Molecular Formula:C₂₀H₃₄N₂O₃Si
Molecular Weight:378.587
Hs Code.:

Synonyms:3-[(1S)-2-[(3S)-3-[(tert-butyldimethylsilyl)oxy]pyrrolidin-1-yl]-1-(methylamino)ethyl]benzoic acid

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Chemical Property of 3-[(1S)-2-[(3S)-3-[(tert-butyldimethylsilyl)oxy]pyrrolidin-1-yl]-1-(methylamino)ethyl]benzoic acid

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Technology Process of 3-[(1S)-2-[(3S)-3-[(tert-butyldimethylsilyl)oxy]pyrrolidin-1-yl]-1-(methylamino)ethyl]benzoic acid

There total 9 articles about 3-[(1S)-2-[(3S)-3-[(tert-butyldimethylsilyl)oxy]pyrrolidin-1-yl]-1-(methylamino)ethyl]benzoic 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:

Reference yield:

: 1455472-89-5
ethyl 3-[(1S)-2-[(3S)-3-[(tert-butyldimethylsilyl)oxy]pyrrolidin-1-yl]-1-(methylamino)ethyl]benzoate

: 1455472-91-9
3-[(1S)-2-[(3S)-3-[(tert-butyldimethylsilyl)oxy]pyrrolidin-1-yl]-1-(methylamino)ethyl]benzoic acid

Guidance literature:: With lithium hydroxide monohydrate; In methanol; water; at 25 ℃; for 1h;

Reference yield:

: 207113-36-8
(S)-3-((tert-butyldimethylsilyl)oxy)pyrrolidine

: 1455472-91-9
3-[(1S)-2-[(3S)-3-[(tert-butyldimethylsilyl)oxy]pyrrolidin-1-yl]-1-(methylamino)ethyl]benzoic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: ethanethiol / 15 h / 70 °C

2.1: triethylamine; methanesulfonyl chloride / dichloromethane / 1.5 h / 0 - 25 °C

2.2: 20 h / 30 °C

3.1: lithium hydroxide monohydrate / water; methanol / 1 h / 25 °C

With lithium hydroxide monohydrate; methanesulfonyl chloride; triethylamine; In methanol; dichloromethane; water; ethanethiol;

Reference yield:

: 3-(2-bromo-acetyl)-benzoic acid ethyl ester

: 1455472-91-9
3-[(1S)-2-[(3S)-3-[(tert-butyldimethylsilyl)oxy]pyrrolidin-1-yl]-1-(methylamino)ethyl]benzoic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: tert-butyl methyl ether; (S)-1-methyl-3,3-diphenyl-hexahydropyrrolo[1,2-c][1,3,2]oxazaborole; N,N-diethylamine-borane / 9 h / 25 - 40 °C

2.1: potassium carbonate / ethanol / 1 h / 0 - 25 °C

3.1: ethanethiol / 15 h / 70 °C

4.1: triethylamine; methanesulfonyl chloride / dichloromethane / 1.5 h / 0 - 25 °C

4.2: 20 h / 30 °C

5.1: lithium hydroxide monohydrate / water; methanol / 1 h / 25 °C

With N,N-diethylamine-borane; lithium hydroxide monohydrate; tert-butyl methyl ether; potassium carbonate; methanesulfonyl chloride; triethylamine; (S)-1-methyl-3,3-diphenyl-hexahydropyrrolo[1,2-c][1,3,2]oxazaborole; In methanol; ethanol; dichloromethane; water; ethanethiol;