(R)-3-Methanesulfonylamino-2-methoxy-pyrrolidine-1-carboxylic acid benzyl ester

Base Information

• Chemical Name: (R)-3-Methanesulfonylamino-2-methoxy-pyrrolidine-1-carboxylic acid benzyl ester
• CAS No.: 1026429-55-9
• Molecular Formula: C₁₄H₂₀N₂O₅S
• Molecular Weight: 328.389
• Mol file: 1026429-55-9.mol

Synonyms:(R)-3-Methanesulfonylamino-2-methoxy-pyrrolidine-1-carboxylic acid benzyl ester

Chemical Property of (R)-3-Methanesulfonylamino-2-methoxy-pyrrolidine-1-carboxylic acid benzyl ester

Chemical Property:

Purity/Quality:

Safty Information:

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Technology Process of (R)-3-Methanesulfonylamino-2-methoxy-pyrrolidine-1-carboxylic acid benzyl ester

There total 1 articles about (R)-3-Methanesulfonylamino-2-methoxy-pyrrolidine-1-carboxylic acid benzyl 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: 99.0%

methanol (67-56-1) + 3-methanesulfonylamino-2-oxo-pyrrolidine-1-carboxylic acid benzyl ester → (R)-3-Methanesulfonylamino-2-methoxy-pyrrolidine-1-carboxylic acid benzyl ester (1026429-55-9)

Guidance literature:

3-methanesulfonylamino-2-oxo-pyrrolidine-1-carboxylic acid benzyl ester; With lithium borohydride; In tetrahydrofuran; at 0 - 20 ℃; for 1h;

methanol; With hydrogenchloride; at 0 - 20 ℃; for 0.75h; Further stages.;

DOI:10.1021/jo001364c

Reference yield: 25.0%

S-(2-pyridinyl) 3-methylbutanethioate (139007-44-6) + (R)-3-Methanesulfonylamino-2-methoxy-pyrrolidine-1-carboxylic acid benzyl ester (1026429-55-9) → (2S,3R)-3-Methanesulfonylamino-2-[(S)-2-methyl-1-(pyridin-2-ylsulfanylcarbonyl)-propyl]-pyrrolidine-1-carboxylic acid benzyl ester (325150-56-9)

Guidance literature:

S-(2-pyridinyl) 3-methylbutanethioate; With titanium tetrachloride; N-ethyl-N,N-diisopropylamine; In dichloromethane;

(R)-3-Methanesulfonylamino-2-methoxy-pyrrolidine-1-carboxylic acid benzyl ester; In dichloromethane; at 0 - 4 ℃; for 1h; Further stages.;

DOI:10.1021/jo001364c

Reference yield:

(R)-3-Methanesulfonylamino-2-methoxy-pyrrolidine-1-carboxylic acid benzyl ester (1026429-55-9) → (3aR,6S,6aS)-6-Isopropyl-4-methanesulfonyl-5-oxo-hexahydro-pyrrolo[3,2-b]pyrrole-1-carboxylic acid benzyl ester (197892-76-5)

Guidance literature:

Multi-step reaction with 2 steps

1.1: TiCl₄; iPr₂NEt / CH₂Cl₂

1.2: 25 percent / CH₂Cl₂ / 1 h / 0 - 4 °C

2.1: 2.05 g / Cs₂CO₃ / CH₂Cl₂ / 20 °C

With titanium tetrachloride; caesium carbonate; N-ethyl-N,N-diisopropylamine; In dichloromethane;

DOI:10.1021/jo001364c

upstream raw materials:

methanol

Downstream raw materials:

(2S,3R)-3-Methanesulfonylamino-2-[(S)-2-methyl-1-(pyridin-2-ylsulfanylcarbonyl)-propyl]-pyrrolidine-1-carboxylic acid benzyl ester

(3aR,6S,6aS)-6-Isopropyl-4-methanesulfonyl-5-oxo-hexahydro-pyrrolo[3,2-b]pyrrole-1-carboxylic acid benzyl ester