(3S,4R,5R)-4-[4-((R)-2-ethoxy-propoxymethyl)-phenyl]-3-formyl-5-[4-(3-methoxy-propyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethoxy]-piperidine-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:(3S,4R,5R)-4-[4-((R)-2-ethoxy-propoxymethyl)-phenyl]-3-formyl-5-[4-(3-methoxy-propyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethoxy]-piperidine-1-carboxylic acid tert-butyl ester
CAS No.:1160437-98-8
Molecular Formula:C₃₆H₅₂N₂O₈
Molecular Weight:640.817
Hs Code.:

(3S,4R,5R)-4-[4-((R)-2-ethoxy-propoxymethyl)-phenyl]-3-formyl-5-[4-(3-methoxy-propyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethoxy]-piperidine-1-carboxylic acid tert-butyl ester

Synonyms:(3S,4R,5R)-4-[4-((R)-2-ethoxy-propoxymethyl)-phenyl]-3-formyl-5-[4-(3-methoxy-propyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethoxy]-piperidine-1-carboxylic acid tert-butyl ester

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Chemical Property of (3S,4R,5R)-4-[4-((R)-2-ethoxy-propoxymethyl)-phenyl]-3-formyl-5-[4-(3-methoxy-propyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethoxy]-piperidine-1-carboxylic acid tert-butyl ester

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Technology Process of (3S,4R,5R)-4-[4-((R)-2-ethoxy-propoxymethyl)-phenyl]-3-formyl-5-[4-(3-methoxy-propyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethoxy]-piperidine-1-carboxylic acid tert-butyl ester

There total 11 articles about (3S,4R,5R)-4-[4-((R)-2-ethoxy-propoxymethyl)-phenyl]-3-formyl-5-[4-(3-methoxy-propyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethoxy]-piperidine-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:

: 1160437-64-8
(3S,4R,5R)-4-[4-((R)-2-ethoxy-propoxymethyl)-phenyl]-3-hydroxymethyl-5-[4-(3-methoxy-propyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethoxy]-piperidine-1-carboxylic acid tert-butyl ester

: 1160437-98-8
(3S,4R,5R)-4-[4-((R)-2-ethoxy-propoxymethyl)-phenyl]-3-formyl-5-[4-(3-methoxy-propyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethoxy]-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: (3S,4R,5R)-4-[4-((R)-2-ethoxy-propoxymethyl)-phenyl]-3-hydroxymethyl-5-[4-(3-methoxy-propyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethoxy]-piperidine-1-carboxylic acid tert-butyl ester; With sulfur trioxide pyridine complex; triethylamine; In dichloromethane; dimethyl sulfoxide; at 0 - 20 ℃;

With potassium hydrogensulfate; In dichloromethane; water; dimethyl sulfoxide;

Reference yield:

: 303043-57-4
(3R,4R,5S)-3-hydroxy-5-hydroxymethyl-4-(4-hydroxy-phenyl)-piperidine-1-carboxylic acid tert-butyl ester

: 1160437-98-8
(3S,4R,5R)-4-[4-((R)-2-ethoxy-propoxymethyl)-phenyl]-3-formyl-5-[4-(3-methoxy-propyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethoxy]-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 10 steps

1.1: triethylamine / dichloromethane / 16 h / 0 - 20 °C

2.1: 1,3-bis-(diphenylphosphino)propane / palladium diacetate / N,N-dimethyl-formamide / 0.33 h / 20 °C

2.2: 4 h / 70 °C / 3750.38 Torr

2.3: 12 h / 70 °C / 3750.38 Torr

3.1: 1H-imidazole / N,N-dimethyl-formamide / 16 h / 20 °C

4.1: tetra-(n-butyl)ammonium iodide; sodium hydride / N,N-dimethyl-formamide; oil / 19 h / -10 - 20 °C

5.1: sodium hydroxide; water / tetrahydrofuran / 16 h / 90 °C

5.2: pH 3

6.1: borane-THF / tetrahydrofuran / 1 - 3 h / 20 °C

7.1: methanesulfonyl chloride; triethylamine / dichloromethane / 16 h / 20 °C

8.1: sodium hydride / N,N-dimethyl-formamide; oil / 19 h / -10 - 20 °C

9.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 1 - 2 h / 20 °C

10.1: sulfur trioxide pyridine complex; triethylamine / dichloromethane; dimethyl sulfoxide / 0 - 20 °C

With 1H-imidazole; sodium hydroxide; borane-THF; 1,3-bis-(diphenylphosphino)propane; tetrabutyl ammonium fluoride; water; sulfur trioxide pyridine complex; tetra-(n-butyl)ammonium iodide; sodium hydride; methanesulfonyl chloride; triethylamine; palladium diacetate; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide; oil;

Reference yield:

: 1160437-84-2
(3R,4R,5S)-3-hydroxy-5-hydroxymethyl-4-(4-trifluoromethanesulfonyloxy-phenyl)-piperidine-1-carboxylic acid tert-butyl ester

: 1160437-98-8
(3S,4R,5R)-4-[4-((R)-2-ethoxy-propoxymethyl)-phenyl]-3-formyl-5-[4-(3-methoxy-propyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-ylmethoxy]-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 9 steps

1.1: 1,3-bis-(diphenylphosphino)propane / palladium diacetate / N,N-dimethyl-formamide / 0.33 h / 20 °C

1.2: 4 h / 70 °C / 3750.38 Torr

1.3: 12 h / 70 °C / 3750.38 Torr

2.1: 1H-imidazole / N,N-dimethyl-formamide / 16 h / 20 °C

3.1: tetra-(n-butyl)ammonium iodide; sodium hydride / N,N-dimethyl-formamide; oil / 19 h / -10 - 20 °C

4.1: sodium hydroxide; water / tetrahydrofuran / 16 h / 90 °C

4.2: pH 3

5.1: borane-THF / tetrahydrofuran / 1 - 3 h / 20 °C

6.1: methanesulfonyl chloride; triethylamine / dichloromethane / 16 h / 20 °C

7.1: sodium hydride / N,N-dimethyl-formamide; oil / 19 h / -10 - 20 °C

8.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 1 - 2 h / 20 °C

9.1: sulfur trioxide pyridine complex; triethylamine / dichloromethane; dimethyl sulfoxide / 0 - 20 °C

With 1H-imidazole; sodium hydroxide; borane-THF; 1,3-bis-(diphenylphosphino)propane; tetrabutyl ammonium fluoride; water; sulfur trioxide pyridine complex; tetra-(n-butyl)ammonium iodide; sodium hydride; methanesulfonyl chloride; triethylamine; palladium diacetate; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide; oil;