3-(2-1H-indol-3-yl-acetoxymethyl)-5-(4-propylbenzoyloxymethyl)-2,3,4,7-tetrahydro-azepine-1-carboxylic acid tert-butyl ester

Base Information

• Chemical Name: 3-(2-1H-indol-3-yl-acetoxymethyl)-5-(4-propylbenzoyloxymethyl)-2,3,4,7-tetrahydro-azepine-1-carboxylic acid tert-butyl ester
• CAS No.: 919106-81-3
• Molecular Formula: C₃₃H₄₀N₂O₆
• Molecular Weight: 560.69
• Mol file: 919106-81-3.mol

Synonyms:3-(2-1H-indol-3-yl-acetoxymethyl)-5-(4-propylbenzoyloxymethyl)-2,3,4,7-tetrahydro-azepine-1-carboxylic acid tert-butyl ester

Chemical Property of 3-(2-1H-indol-3-yl-acetoxymethyl)-5-(4-propylbenzoyloxymethyl)-2,3,4,7-tetrahydro-azepine-1-carboxylic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3-(2-1H-indol-3-yl-acetoxymethyl)-5-(4-propylbenzoyloxymethyl)-2,3,4,7-tetrahydro-azepine-1-carboxylic acid tert-butyl ester

There total 5 articles about 3-(2-1H-indol-3-yl-acetoxymethyl)-5-(4-propylbenzoyloxymethyl)-2,3,4,7-tetrahydro-azepine-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%

5-hydroxymethyl-3-(2-1H-indol-3-yl-acetoxymethyl)-2,3,4,7-tetrahydro-azepine-1-carboxylic acid tert-butyl ester (919106-76-6) + 4-propylbenzoyl chloride (52710-27-7) → 3-(2-1H-indol-3-yl-acetoxymethyl)-5-(4-propylbenzoyloxymethyl)-2,3,4,7-tetrahydro-azepine-1-carboxylic acid tert-butyl ester (919106-81-3)

Guidance literature:

With dmap; In dichloromethane; at 20 ℃; for 14h;

DOI:10.1016/j.jorganchem.2006.09.031

Reference yield:

2-[(allyl-tert-butoxycarbonyl-amino)-methyl]-4-(tert-butyl-dimethyl-silanyloxymethyl)-pent-4-enoic acid methyl ester (881398-74-9) → 3-(2-1H-indol-3-yl-acetoxymethyl)-5-(4-propylbenzoyloxymethyl)-2,3,4,7-tetrahydro-azepine-1-carboxylic acid tert-butyl ester (919106-81-3)

Guidance literature:

Multi-step reaction with 5 steps

1: 83 percent / Grubbs 2 catalyst / CH₂Cl₂ / 8 h / 40 °C

2: 76 percent / DIBAL-H / toluene; tetrahydrofuran / 3 h / -78 °C

3: 82 percent / DMAP; DCC / tetrahydrofuran; CH₂Cl₂ / 14 h / 20 °C

4: 85 percent / aq. HCl / tetrahydrofuran / 0.67 h / 20 °C

5: 61 percent / DMAP / CH₂Cl₂ / 14 h / 20 °C

With hydrogenchloride; dmap; diisobutylaluminium hydride; dicyclohexyl-carbodiimide; tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; In tetrahydrofuran; dichloromethane; toluene;

DOI:10.1016/j.jorganchem.2006.09.031

Reference yield:

5-(tert-butyl-dimethyl-silanyloxymethyl)-2,3,4,7-tetrahydro-1H-azepine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester (881398-84-1) → 3-(2-1H-indol-3-yl-acetoxymethyl)-5-(4-propylbenzoyloxymethyl)-2,3,4,7-tetrahydro-azepine-1-carboxylic acid tert-butyl ester (919106-81-3)

Guidance literature:

Multi-step reaction with 4 steps

1: 76 percent / DIBAL-H / toluene; tetrahydrofuran / 3 h / -78 °C

2: 82 percent / DMAP; DCC / tetrahydrofuran; CH₂Cl₂ / 14 h / 20 °C

3: 85 percent / aq. HCl / tetrahydrofuran / 0.67 h / 20 °C

4: 61 percent / DMAP / CH₂Cl₂ / 14 h / 20 °C

With hydrogenchloride; dmap; diisobutylaluminium hydride; dicyclohexyl-carbodiimide; In tetrahydrofuran; dichloromethane; toluene;

DOI:10.1016/j.jorganchem.2006.09.031

upstream raw materials:

5-hydroxymethyl-3-(2-1H-indol-3-yl-acetoxymethyl)-2,3,4,7-tetrahydro-azepine-1-carboxylic acid tert-butyl ester

4-propylbenzoyl chloride

5-(tert-butyl-dimethyl-silanyloxymethyl)-2,3,4,7-tetrahydro-1H-azepine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester

2-[(allyl-tert-butoxycarbonyl-amino)-methyl]-4-(tert-butyl-dimethyl-silanyloxymethyl)-pent-4-enoic acid methyl ester