(2R,5S)-2-Benzyloxymethyl-5-[8-methoxy-1-((4S,5S)-5-methoxymethoxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-isoquinolin-3-yl]-pyrrolidine-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:(2R,5S)-2-Benzyloxymethyl-5-[8-methoxy-1-((4S,5S)-5-methoxymethoxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-isoquinolin-3-yl]-pyrrolidine-1-carboxylic acid tert-butyl ester
CAS No.:159571-68-3
Molecular Formula:C₃₅H₄₆N₂O₈
Molecular Weight:622.759
Hs Code.:

(2R,5S)-2-Benzyloxymethyl-5-[8-methoxy-1-((4S,5S)-5-methoxymethoxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-isoquinolin-3-yl]-pyrrolidine-1-carboxylic acid tert-butyl ester

Synonyms:(2R,5S)-2-Benzyloxymethyl-5-[8-methoxy-1-((4S,5S)-5-methoxymethoxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-isoquinolin-3-yl]-pyrrolidine-1-carboxylic acid tert-butyl ester

Suppliers and Price of (2R,5S)-2-Benzyloxymethyl-5-[8-methoxy-1-((4S,5S)-5-methoxymethoxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-isoquinolin-3-yl]-pyrrolidine-1-carboxylic acid tert-butyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (2R,5S)-2-Benzyloxymethyl-5-[8-methoxy-1-((4S,5S)-5-methoxymethoxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-isoquinolin-3-yl]-pyrrolidine-1-carboxylic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2R,5S)-2-Benzyloxymethyl-5-[8-methoxy-1-((4S,5S)-5-methoxymethoxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-isoquinolin-3-yl]-pyrrolidine-1-carboxylic acid tert-butyl ester

There total 8 articles about (2R,5S)-2-Benzyloxymethyl-5-[8-methoxy-1-((4S,5S)-5-methoxymethoxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-isoquinolin-3-yl]-pyrrolidine-1-carboxylic acid tert-butyl 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: 61.0%

: 159571-67-2
(2R,5S)-2-Benzyloxymethyl-5-{2-[3-methoxy-2-((4R,5S)-5-methoxymethoxymethyl-2,2-dimethyl-[1,3]dioxolane-4-carbonyl)-phenyl]-acetyl}-pyrrolidine-1-carboxylic acid tert-butyl ester

: 159571-68-3
(2R,5S)-2-Benzyloxymethyl-5-[8-methoxy-1-((4S,5S)-5-methoxymethoxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-isoquinolin-3-yl]-pyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:: With ammonium hydroxide; In tetrahydrofuran; water; for 15h; Ambient temperature;
DOI:10.1016/S0040-4020(01)80644-X

Reference yield:

: 38197-43-2
2-bromo-3-methylanisole

: 159571-68-3
(2R,5S)-2-Benzyloxymethyl-5-[8-methoxy-1-((4S,5S)-5-methoxymethoxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-isoquinolin-3-yl]-pyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 95 percent / n-butyllihium / hexane; diethyl ether / 0.75 h / -78 °C

2: 97 percent / pyridine, chromium (VI) oxide / CH₂Cl₂ / 0.75 h / Ambient temperature

3: 94 percent / hydrogen / 20percent Pd/C / methanol / 15 h / 760 Torr / Ambient temperature

4: 94 percent / N,N-diisopropylethylamine / CH₂Cl₂ / 17 h / Ambient temperature

5: 48 percent / lithium diisopropylamide, N,N,N',N'-tetramethylethylenediamine / tetrahydrofuran; hexane / 2 h / -78 °C

6: 61 percent / 2.6 M Jones reagent, celite / acetone / 0.33 h / Ambient temperature

7: 61 percent / 38percent ammonia / H₂O; tetrahydrofuran / 15 h / Ambient temperature

With pyridine; chromium(VI) oxide; ammonium hydroxide; n-butyllithium; jones reagent; N,N,N,N,-tetramethylethylenediamine; Celite; hydrogen; N-ethyl-N,N-diisopropylamine; lithium diisopropyl amide; palladium on activated charcoal; In tetrahydrofuran; methanol; diethyl ether; hexane; dichloromethane; water; acetone;
DOI:10.1016/S0040-4020(01)80644-X

Reference yield:

: 81028-12-8
(4S,5R)-4-benzyloxymethyl-2,2-dimethyl-1,3-dioxolane-5-carboxaldehyde

: 159571-68-3
(2R,5S)-2-Benzyloxymethyl-5-[8-methoxy-1-((4S,5S)-5-methoxymethoxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-isoquinolin-3-yl]-pyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 95 percent / n-butyllihium / hexane; diethyl ether / 0.75 h / -78 °C

2: 97 percent / pyridine, chromium (VI) oxide / CH₂Cl₂ / 0.75 h / Ambient temperature

3: 94 percent / hydrogen / 20percent Pd/C / methanol / 15 h / 760 Torr / Ambient temperature

4: 94 percent / N,N-diisopropylethylamine / CH₂Cl₂ / 17 h / Ambient temperature

5: 48 percent / lithium diisopropylamide, N,N,N',N'-tetramethylethylenediamine / tetrahydrofuran; hexane / 2 h / -78 °C

6: 61 percent / 2.6 M Jones reagent, celite / acetone / 0.33 h / Ambient temperature

7: 61 percent / 38percent ammonia / H₂O; tetrahydrofuran / 15 h / Ambient temperature

With pyridine; chromium(VI) oxide; ammonium hydroxide; n-butyllithium; jones reagent; N,N,N,N,-tetramethylethylenediamine; Celite; hydrogen; N-ethyl-N,N-diisopropylamine; lithium diisopropyl amide; palladium on activated charcoal; In tetrahydrofuran; methanol; diethyl ether; hexane; dichloromethane; water; acetone;
DOI:10.1016/S0040-4020(01)80644-X