[(3R,5S)-5-(((1R,2R)-1-(cyclopropylsulfonylcarbamoyl)-2-ethylcyclopropyl)carbamoyl)-1-((S)-2-(tert-butoxycarbonyl)-2-cyclohexylacetyl)pyrrolidin-3-yl] 4-chloroisoindoline-2-carboxylate

Base Information

Chemical Name:[(3R,5S)-5-(((1R,2R)-1-(cyclopropylsulfonylcarbamoyl)-2-ethylcyclopropyl)carbamoyl)-1-((S)-2-(tert-butoxycarbonyl)-2-cyclohexylacetyl)pyrrolidin-3-yl] 4-chloroisoindoline-2-carboxylate
CAS No.:1083092-37-8
Molecular Formula:C₃₆H₅₀ClN₅O₉S
Molecular Weight:764.34
Hs Code.:

[(3R,5S)-5-(((1R,2R)-1-(cyclopropylsulfonylcarbamoyl)-2-ethylcyclopropyl)carbamoyl)-1-((S)-2-(tert-butoxycarbonyl)-2-cyclohexylacetyl)pyrrolidin-3-yl] 4-chloroisoindoline-2-carboxylate

Synonyms:[(3R,5S)-5-(((1R,2R)-1-(cyclopropylsulfonylcarbamoyl)-2-ethylcyclopropyl)carbamoyl)-1-((S)-2-(tert-butoxycarbonyl)-2-cyclohexylacetyl)pyrrolidin-3-yl] 4-chloroisoindoline-2-carboxylate

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Chemical Property of [(3R,5S)-5-(((1R,2R)-1-(cyclopropylsulfonylcarbamoyl)-2-ethylcyclopropyl)carbamoyl)-1-((S)-2-(tert-butoxycarbonyl)-2-cyclohexylacetyl)pyrrolidin-3-yl] 4-chloroisoindoline-2-carboxylate

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Technology Process of [(3R,5S)-5-(((1R,2R)-1-(cyclopropylsulfonylcarbamoyl)-2-ethylcyclopropyl)carbamoyl)-1-((S)-2-(tert-butoxycarbonyl)-2-cyclohexylacetyl)pyrrolidin-3-yl] 4-chloroisoindoline-2-carboxylate

There total 10 articles about [(3R,5S)-5-(((1R,2R)-1-(cyclopropylsulfonylcarbamoyl)-2-ethylcyclopropyl)carbamoyl)-1-((S)-2-(tert-butoxycarbonyl)-2-cyclohexylacetyl)pyrrolidin-3-yl] 4-chloroisoindoline-2-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: 95.0%

: 1083091-90-0
(3R,5S)-5-((1R,2R)-1-(cyclopropylsulfonylcarbamoyl)-2-ethylcyclopropylcarbamoyl)pyrrolidin-3-yl 4-chloroisoindoline-2-carboxylate hydrochloride

: 109183-71-3
N-(tert-butoxycarbonyl)-L-cyclohexylglycine

: 1083092-37-8
[(3R,5S)-5-(((1R,2R)-1-(cyclopropylsulfonylcarbamoyl)-2-ethylcyclopropyl)carbamoyl)-1-((S)-2-(tert-butoxycarbonyl)-2-cyclohexylacetyl)pyrrolidin-3-yl] 4-chloroisoindoline-2-carboxylate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 17h;

Reference yield:

: 159622-10-3,213316-50-8,259221-77-7
(1R,2S)-1-(tert-butoxycarbonylamino)-2-vinylcyclopropanecarboxylic acid

: 1083092-37-8
[(3R,5S)-5-(((1R,2R)-1-(cyclopropylsulfonylcarbamoyl)-2-ethylcyclopropyl)carbamoyl)-1-((S)-2-(tert-butoxycarbonyl)-2-cyclohexylacetyl)pyrrolidin-3-yl] 4-chloroisoindoline-2-carboxylate

Guidance literature:: Multi-step reaction with 6 steps

1.1: hydrogen / palladium hydroxide on carbon / tert-butyl methyl ether / 5 h / 20 °C / 760.05 Torr

2.1: 1,1'-carbonyldiimidazole / tetrahydrofuran / 4 h / 20 - 60 °C

2.2: 20 °C

3.1: hydrogenchloride / 1,4-dioxane / 5 h / 20 °C

4.1: N-ethyl-N,N-diisopropylamine; HATU / dichloromethane / 18 h / 20 °C

4.2: pH 3 - 4

5.1: hydrogenchloride / 1,4-dioxane; dichloromethane / 2 h / 20 °C

6.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 17 h / 0 - 20 °C

With hydrogenchloride; hydrogen; N-ethyl-N,N-diisopropylamine; HATU; 1,1'-carbonyldiimidazole; palladium hydroxide on carbon; In tetrahydrofuran; 1,4-dioxane; dichloromethane; tert-butyl methyl ether; N,N-dimethyl-formamide;

Reference yield:

: 923591-34-8
tert-butyl ((1R,2R)-1-{[(cyclopropylsulfonyl)amino]carbonyl}-2-ethylcyclopropyl)carbamate

: 1083092-37-8
[(3R,5S)-5-(((1R,2R)-1-(cyclopropylsulfonylcarbamoyl)-2-ethylcyclopropyl)carbamoyl)-1-((S)-2-(tert-butoxycarbonyl)-2-cyclohexylacetyl)pyrrolidin-3-yl] 4-chloroisoindoline-2-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogenchloride / 1,4-dioxane / 5 h / 20 °C

2.1: N-ethyl-N,N-diisopropylamine; HATU / dichloromethane / 18 h / 20 °C

2.2: pH 3 - 4

3.1: hydrogenchloride / 1,4-dioxane; dichloromethane / 2 h / 20 °C

4.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 17 h / 0 - 20 °C

With hydrogenchloride; N-ethyl-N,N-diisopropylamine; HATU; In 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide;