1S,2R,5S-menthyl r-2S-methoxycarbonyl-2-phenyl-c-5S-(4'-iodo-N-phenylsuphonylindol-3'-yl)pyrrolidine-c-4R-carboxylate

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Chemical Name:1S,2R,5S-menthyl r-2S-methoxycarbonyl-2-phenyl-c-5S-(4'-iodo-N-phenylsuphonylindol-3'-yl)pyrrolidine-c-4R-carboxylate
CAS No.:161201-97-4
Molecular Formula:C₃₇H₄₁IN₂O₆S
Molecular Weight:768.713
Hs Code.:

Synonyms:1S,2R,5S-menthyl r-2S-methoxycarbonyl-2-phenyl-c-5S-(4'-iodo-N-phenylsuphonylindol-3'-yl)pyrrolidine-c-4R-carboxylate

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Chemical Property of 1S,2R,5S-menthyl r-2S-methoxycarbonyl-2-phenyl-c-5S-(4'-iodo-N-phenylsuphonylindol-3'-yl)pyrrolidine-c-4R-carboxylate

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Technology Process of 1S,2R,5S-menthyl r-2S-methoxycarbonyl-2-phenyl-c-5S-(4'-iodo-N-phenylsuphonylindol-3'-yl)pyrrolidine-c-4R-carboxylate

There total 3 articles about 1S,2R,5S-menthyl r-2S-methoxycarbonyl-2-phenyl-c-5S-(4'-iodo-N-phenylsuphonylindol-3'-yl)pyrrolidine-c-4R-carboxylate 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: 80.0%

: 108945-28-4
(1S,2R,5S)‐2‐isopropyl‐5‐methylcyclohexyl acrylate

: methyl N-(4-iodo-N-phenylsulphonylindolyl-3-methylidene)-phenylglycinate

: 161201-97-4
1S,2R,5S-menthyl r-2S-methoxycarbonyl-2-phenyl-c-5S-(4'-iodo-N-phenylsuphonylindol-3'-yl)pyrrolidine-c-4R-carboxylate

Guidance literature:: With N,N,N′,N′-tetramethyl-N″-tert-butylguanidine; lithium bromide; In acetonitrile; for 2h; Ambient temperature;
DOI:10.1016/0040-4020(94)00956-U

Reference yield:

: 15028-40-7,13226-98-7
DL-2-phenylglycine methyl ester hydrochloride

: 161201-97-4
1S,2R,5S-menthyl r-2S-methoxycarbonyl-2-phenyl-c-5S-(4'-iodo-N-phenylsuphonylindol-3'-yl)pyrrolidine-c-4R-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / MgSO₄, triethylamine / CH₂Cl₂ / 12 h / Ambient temperature

2: 80 percent / LiBr, 2-t-butyl tetramethylguanidine / acetonitrile / 2 h / Ambient temperature

With N,N,N′,N′-tetramethyl-N″-tert-butylguanidine; magnesium sulfate; triethylamine; lithium bromide; In dichloromethane; acetonitrile;
DOI:10.1016/0040-4020(94)00956-U

Reference yield:

: 1-Benzenesulfonyl-4-iodo-1H-indole-3-carbaldehyde

: 161201-97-4
1S,2R,5S-menthyl r-2S-methoxycarbonyl-2-phenyl-c-5S-(4'-iodo-N-phenylsuphonylindol-3'-yl)pyrrolidine-c-4R-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / MgSO₄, triethylamine / CH₂Cl₂ / 12 h / Ambient temperature

2: 80 percent / LiBr, 2-t-butyl tetramethylguanidine / acetonitrile / 2 h / Ambient temperature

With N,N,N′,N′-tetramethyl-N″-tert-butylguanidine; magnesium sulfate; triethylamine; lithium bromide; In dichloromethane; acetonitrile;
DOI:10.1016/0040-4020(94)00956-U