(2S,3S)-1-Benzoyl-4-(3,4-bis-benzyloxy-2-methoxy-phenyl)-3-tert-butoxycarbonylmethyl-2,3-dihydro-1H-pyrrole-2-carboxylic acid methyl ester

Base Information

Chemical Name:(2S,3S)-1-Benzoyl-4-(3,4-bis-benzyloxy-2-methoxy-phenyl)-3-tert-butoxycarbonylmethyl-2,3-dihydro-1H-pyrrole-2-carboxylic acid methyl ester
CAS No.:210824-83-2
Molecular Formula:C₄₀H₄₁NO₈
Molecular Weight:663.767
Hs Code.:

Synonyms:(2S,3S)-1-Benzoyl-4-(3,4-bis-benzyloxy-2-methoxy-phenyl)-3-tert-butoxycarbonylmethyl-2,3-dihydro-1H-pyrrole-2-carboxylic acid methyl ester

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Chemical Property of (2S,3S)-1-Benzoyl-4-(3,4-bis-benzyloxy-2-methoxy-phenyl)-3-tert-butoxycarbonylmethyl-2,3-dihydro-1H-pyrrole-2-carboxylic acid methyl ester

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Technology Process of (2S,3S)-1-Benzoyl-4-(3,4-bis-benzyloxy-2-methoxy-phenyl)-3-tert-butoxycarbonylmethyl-2,3-dihydro-1H-pyrrole-2-carboxylic acid methyl ester

There total 4 articles about (2S,3S)-1-Benzoyl-4-(3,4-bis-benzyloxy-2-methoxy-phenyl)-3-tert-butoxycarbonylmethyl-2,3-dihydro-1H-pyrrole-2-carboxylic acid methyl 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:

: 934-00-9
3-methocycatechol

: 210824-83-2
(2S,3S)-1-Benzoyl-4-(3,4-bis-benzyloxy-2-methoxy-phenyl)-3-tert-butoxycarbonylmethyl-2,3-dihydro-1H-pyrrole-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 91 percent / K₂CO₃ / dimethylformamide / 24 h / Ambient temperature

2: 50 percent / N-bromosucciminide / CCl₄ / 24 h / Ambient temperature

3: 1.) n-BuLi, 2.) B(OMe)3, 3.) aq. Na₂CO₃, LiCl / 3.) Pd(PPh₃)4 / 1.) THF, pentane, -78 deg C, 50 min, 2.) 1 h, 3.) DME, reflux, 40 min

With N-Bromosuccinimide; n-butyllithium; Trimethyl borate; sodium carbonate; potassium carbonate; lithium chloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrachloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4020(98)00377-9

Reference yield:

: 55020-67-2
1,2-bis-benzyloxy-3-methoxy-benzene

: 210824-83-2
(2S,3S)-1-Benzoyl-4-(3,4-bis-benzyloxy-2-methoxy-phenyl)-3-tert-butoxycarbonylmethyl-2,3-dihydro-1H-pyrrole-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 50 percent / N-bromosucciminide / CCl₄ / 24 h / Ambient temperature

2: 1.) n-BuLi, 2.) B(OMe)3, 3.) aq. Na₂CO₃, LiCl / 3.) Pd(PPh₃)4 / 1.) THF, pentane, -78 deg C, 50 min, 2.) 1 h, 3.) DME, reflux, 40 min

With N-Bromosuccinimide; n-butyllithium; Trimethyl borate; sodium carbonate; lithium chloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrachloromethane;
DOI:10.1016/S0040-4020(98)00377-9

Reference yield:

: 100-39-0
benzyl bromide

: 210824-83-2
(2S,3S)-1-Benzoyl-4-(3,4-bis-benzyloxy-2-methoxy-phenyl)-3-tert-butoxycarbonylmethyl-2,3-dihydro-1H-pyrrole-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 91 percent / K₂CO₃ / dimethylformamide / 24 h / Ambient temperature

2: 50 percent / N-bromosucciminide / CCl₄ / 24 h / Ambient temperature

3: 1.) n-BuLi, 2.) B(OMe)3, 3.) aq. Na₂CO₃, LiCl / 3.) Pd(PPh₃)4 / 1.) THF, pentane, -78 deg C, 50 min, 2.) 1 h, 3.) DME, reflux, 40 min

With N-Bromosuccinimide; n-butyllithium; Trimethyl borate; sodium carbonate; potassium carbonate; lithium chloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrachloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4020(98)00377-9