(2R,3aR,7aR)-1-[(S)-2-((S)-1-Carboxy-3-phenyl-propylamino)-propionyl]-octahydro-indole-2-carboxylic acid

Base Information

• Chemical Name: (2R,3aR,7aR)-1-[(S)-2-((S)-1-Carboxy-3-phenyl-propylamino)-propionyl]-octahydro-indole-2-carboxylic acid
• CAS No.: 80876-05-7
• Molecular Formula: C₂₂H₃₀N₂O₅
• Molecular Weight: 402.491
• Mol file: 80876-05-7.mol

Synonyms:(2R,3aR,7aR)-1-[(S)-2-((S)-1-Carboxy-3-phenyl-propylamino)-propionyl]-octahydro-indole-2-carboxylic acid

Chemical Property of (2R,3aR,7aR)-1-[(S)-2-((S)-1-Carboxy-3-phenyl-propylamino)-propionyl]-octahydro-indole-2-carboxylic acid

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (2R,3aR,7aR)-1-[(S)-2-((S)-1-Carboxy-3-phenyl-propylamino)-propionyl]-octahydro-indole-2-carboxylic acid

There total 7 articles about (2R,3aR,7aR)-1-[(S)-2-((S)-1-Carboxy-3-phenyl-propylamino)-propionyl]-octahydro-indole-2-carboxylic acid 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:

(+/-)-(2S,3aS,7aS)-octahydroindole-2-carboxylic acid (80828-13-3,80875-98-5,82717-40-6,87679-20-7,87679-39-8,87679-51-4,87679-58-1,88547-85-7,88585-94-8,96844-78-9,108507-42-2,145438-94-4,145438-95-5,145513-90-2,145513-91-3,145513-92-4,145513-93-5,2055118-14-2) → (2R,3aR,7aR)-1-[(S)-2-((S)-1-Carboxy-3-phenyl-propylamino)-propionyl]-octahydro-indole-2-carboxylic acid (80876-05-7)

Guidance literature:

Multi-step reaction with 5 steps

1: 76 percent / conc. H₂SO₄ / dioxane / 20 h / 20 °C

3: 1-hydroxybenzotriazole, N,N'-dicyclohexylcarbodiimide / tetrahydrofuran / a) 0 deg C, 1 h, b) RT, overnight

4: HCl(g) / CH₂Cl₂ / 0 °C

5: NaOH / H₂O / Ambient temperature

With hydrogenchloride; sodium hydroxide; sulfuric acid; benzotriazol-1-ol; dicyclohexyl-carbodiimide; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water;

DOI:10.1021/jm00389a006

Reference yield:

2-carbethoxyindole (3770-50-1,117770-52-2) → (2R,3aR,7aR)-1-[(S)-2-((S)-1-Carboxy-3-phenyl-propylamino)-propionyl]-octahydro-indole-2-carboxylic acid (80876-05-7)

Guidance literature:

Multi-step reaction with 7 steps

1: H₂ / Rh/C / acetic acid

2: aq. 15percent HCl / 4 h / Heating

3: 76 percent / conc. H₂SO₄ / dioxane / 20 h / 20 °C

5: 1-hydroxybenzotriazole, N,N'-dicyclohexylcarbodiimide / tetrahydrofuran / a) 0 deg C, 1 h, b) RT, overnight

6: HCl(g) / CH₂Cl₂ / 0 °C

7: NaOH / H₂O / Ambient temperature

With hydrogenchloride; sodium hydroxide; sulfuric acid; hydrogen; benzotriazol-1-ol; dicyclohexyl-carbodiimide; Rh on carbon; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water; acetic acid;

DOI:10.1021/jm00389a006

Reference yield:

(2S,3aS,7aS)-Octahydro-indole-2-carboxylic acid ethyl ester (79799-08-9,80828-11-1,89083-53-4,111821-02-4) → (2R,3aR,7aR)-1-[(S)-2-((S)-1-Carboxy-3-phenyl-propylamino)-propionyl]-octahydro-indole-2-carboxylic acid (80876-05-7)

Guidance literature:

Multi-step reaction with 6 steps

1: aq. 15percent HCl / 4 h / Heating

2: 76 percent / conc. H₂SO₄ / dioxane / 20 h / 20 °C

4: 1-hydroxybenzotriazole, N,N'-dicyclohexylcarbodiimide / tetrahydrofuran / a) 0 deg C, 1 h, b) RT, overnight

5: HCl(g) / CH₂Cl₂ / 0 °C

6: NaOH / H₂O / Ambient temperature

With hydrogenchloride; sodium hydroxide; sulfuric acid; benzotriazol-1-ol; dicyclohexyl-carbodiimide; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water;

DOI:10.1021/jm00389a006

upstream raw materials:

(2R,3aR,7aR)-1-[(S)-2-((S)-1-Ethoxycarbonyl-3-phenyl-propylamino)-propionyl]-octahydro-indole-2-carboxylic acid

2-carbethoxyindole

(+/-)-(2S,3aS,7aS)-octahydroindole-2-carboxylic acid

(2S,3aS,7aS)-Octahydro-indole-2-carboxylic acid ethyl ester