(2S,4S)-2-(Methanesulfonylamino-methyl)-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid 4-methoxy-benzyl ester

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Chemical Name:(2S,4S)-2-(Methanesulfonylamino-methyl)-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid 4-methoxy-benzyl ester
CAS No.:175846-16-9
Molecular Formula:C₃₄H₃₆N₂O₅S₂
Molecular Weight:616.802
Hs Code.:

Synonyms:(2S,4S)-2-(Methanesulfonylamino-methyl)-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid 4-methoxy-benzyl ester

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Chemical Property of (2S,4S)-2-(Methanesulfonylamino-methyl)-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid 4-methoxy-benzyl ester

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Technology Process of (2S,4S)-2-(Methanesulfonylamino-methyl)-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid 4-methoxy-benzyl ester

There total 9 articles about (2S,4S)-2-(Methanesulfonylamino-methyl)-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid 4-methoxy-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: 100.0%

: 124-63-0
methanesulfonyl chloride

: 148016-92-6
(2S,4S)-2-aminomethyl-1-p-methoxybenzyloxycarbonyl-4-tritylthiopyrrolidine

: 175846-16-9
(2S,4S)-2-(Methanesulfonylamino-methyl)-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid 4-methoxy-benzyl ester

Guidance literature:: With triethylamine; In dichloromethane; at -30 ℃; for 0.333333h;
DOI:10.7164/antibiotics.49.199

Reference yield:

: 1499-56-5,775275-31-5,790644-51-8,754962-86-2
(R)-4-hydroxy-L-proline ethyl ester

: 175846-16-9
(2S,4S)-2-(Methanesulfonylamino-methyl)-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid 4-methoxy-benzyl ester

Guidance literature:: Multi-step reaction with 8 steps

1: 32.48 g / triethylamine / methanol / 0.33 h

2: 98 percent / triethylamine / CH₂Cl₂ / 0.25 h / -30 °C

3: 1) sodium hydride / 1) DMF, room temperature, 1 h, 2) 60 deg C, 30 min

4: 68 percent / LiBH₄ / tetrahydrofuran / 0.5 h / 60 °C

5: 87.4 percent / triethylamine / CH₂Cl₂ / 0.33 h / -30 °C

6: 78.1 percent / dimethylformamide / 1 h / 100 °C

7: 78 percent / H₂NNH₂*H₂O / CH₂Cl₂; methanol / 5 h / 60 °C

8: 100 percent / triethylamine / CH₂Cl₂ / 0.33 h / -30 °C

With lithium borohydride; sodium hydride; hydrazine hydrate; triethylamine; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.7164/antibiotics.49.199

Reference yield:

: 104773-44-6
(2S,4R)-1-p-methoxybenzyloxycarbonyl-4-hydroxypyrrolidine-2-carboxylic acid methyl ester

: 175846-16-9
(2S,4S)-2-(Methanesulfonylamino-methyl)-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid 4-methoxy-benzyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 98 percent / triethylamine / CH₂Cl₂ / 0.25 h / -30 °C

2: 1) sodium hydride / 1) DMF, room temperature, 1 h, 2) 60 deg C, 30 min

3: 68 percent / LiBH₄ / tetrahydrofuran / 0.5 h / 60 °C

4: 87.4 percent / triethylamine / CH₂Cl₂ / 0.33 h / -30 °C

5: 78.1 percent / dimethylformamide / 1 h / 100 °C

6: 78 percent / H₂NNH₂*H₂O / CH₂Cl₂; methanol / 5 h / 60 °C

7: 100 percent / triethylamine / CH₂Cl₂ / 0.33 h / -30 °C

With lithium borohydride; sodium hydride; hydrazine hydrate; triethylamine; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.7164/antibiotics.49.199