2-(2-benzyloxycarbonylamino-ethyl)-3-methanesulfonyloxy-pyrrolidine-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:2-(2-benzyloxycarbonylamino-ethyl)-3-methanesulfonyloxy-pyrrolidine-1-carboxylic acid tert-butyl ester
CAS No.:1218931-24-8
Molecular Formula:C₂₀H₃₀N₂O₇S
Molecular Weight:442.533
Hs Code.:

Synonyms:2-(2-benzyloxycarbonylamino-ethyl)-3-methanesulfonyloxy-pyrrolidine-1-carboxylic acid tert-butyl ester

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Chemical Property of 2-(2-benzyloxycarbonylamino-ethyl)-3-methanesulfonyloxy-pyrrolidine-1-carboxylic acid tert-butyl ester

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Technology Process of 2-(2-benzyloxycarbonylamino-ethyl)-3-methanesulfonyloxy-pyrrolidine-1-carboxylic acid tert-butyl ester

There total 8 articles about 2-(2-benzyloxycarbonylamino-ethyl)-3-methanesulfonyloxy-pyrrolidine-1-carboxylic acid tert-butyl ester 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: 100.0%

: 1218931-23-7
2-(2-benzyloxycarbonylamino-ethyl)-3-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester

: 124-63-0
methanesulfonyl chloride

: 1218931-24-8
2-(2-benzyloxycarbonylamino-ethyl)-3-methanesulfonyloxy-pyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 ℃; for 1h;

Reference yield:

: 757247-71-5
tert-butyl (2S,3S)-3-{[tert-butyl(dimethyl)silyl]oxy}-2-formylpyrrolidine-1-carboxylate

: 1218931-24-8
2-(2-benzyloxycarbonylamino-ethyl)-3-methanesulfonyloxy-pyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: triethylamine / 12 h

1.2: 1 h / -78 °C

1.3: 1 h / -78 °C

2.1: sodium tetrahydroborate; water / tetrahydrofuran / 2 h / 20 °C

3.1: hydrogen / ethanol; water / 2 h / 2844.39 Torr

3.2: 16 h / 0 - 20 °C

4.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 16 h / 0 - 20 °C

5.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / 0 °C

With sodium tetrahydroborate; tetrabutyl ammonium fluoride; water; hydrogen; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; ethanol; dichloromethane; water;

Reference yield:

: 184046-78-4
(2S,3S)-1-tert-butyl-2-methyl 3-hydroxypyrrolidine-1,2-dicarboxylate

: 1218931-24-8
2-(2-benzyloxycarbonylamino-ethyl)-3-methanesulfonyloxy-pyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 8 steps

1.1: 1H-imidazole / dichloromethane / 6 h / 0 - 20 °C

2.1: lithium borohydride / tetrahydrofuran / 0 - 20 °C

3.1: pyridine-SO₃ complex; triethylamine / dichloromethane; dimethyl sulfoxide / 2 h / 0 - 20 °C

4.1: triethylamine / 12 h

4.2: 1 h / -78 °C

4.3: 1 h / -78 °C

5.1: sodium tetrahydroborate; water / tetrahydrofuran / 2 h / 20 °C

6.1: hydrogen / ethanol; water / 2 h / 2844.39 Torr

6.2: 16 h / 0 - 20 °C

7.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 16 h / 0 - 20 °C

8.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 1 h / 0 °C

With 1H-imidazole; sodium tetrahydroborate; lithium borohydride; pyridine-SO₃ complex; tetrabutyl ammonium fluoride; water; hydrogen; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; ethanol; dichloromethane; water; dimethyl sulfoxide;