phenylmethyl -<2-<<3-(1H-indol-3-yl)-2-methyl-2-<(5-oxo-spiro3,5>octan>-2-yl)-amino>propyl>amino>-1-phenylethyl>carbamate

Base Information

• Chemical Name: phenylmethyl -<2-<<3-(1H-indol-3-yl)-2-methyl-2-<(5-oxo-spiro3,5>octan>-2-yl)-amino>propyl>amino>-1-phenylethyl>carbamate
• CAS No.: 144876-81-3
• Molecular Formula: C₄₀H₄₃N₅O₅
• Molecular Weight: 673.812
• Mol file: 144876-81-3.mol

Synonyms:phenylmethyl -<2-<<3-(1H-indol-3-yl)-2-methyl-2-<(5-oxo-spiro3,5>octan>-2-yl)-amino>propyl>amino>-1-phenylethyl>carbamate

Chemical Property of phenylmethyl -<2-<<3-(1H-indol-3-yl)-2-methyl-2-<(5-oxo-spiro3,5>octan>-2-yl)-amino>propyl>amino>-1-phenylethyl>carbamate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of phenylmethyl -<2-<<3-(1H-indol-3-yl)-2-methyl-2-<(5-oxo-spiro3,5>octan>-2-yl)-amino>propyl>amino>-1-phenylethyl>carbamate

There total 10 articles about phenylmethyl -<2-<<3-(1H-indol-3-yl)-2-methyl-2-<(5-oxo-spiro3,5>octan>-2-yl)-amino>propyl>amino>-1-phenylethyl>carbamate 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%

phenylmethyl-4-(1H-indol-3-ylmethyl)-1-<2-(methoxycarbonyl)tricyclo<3.3.1.13,7>-dec-2-yl>-4-methyl-2,5-dioxo-8-phenyl-1,3,6,9-tetraazadecan-10-oate (144876-73-3) → phenylmethyl -<2-<<3-(1H-indol-3-yl)-2-methyl-2-<(5-oxo-spiro3,5>octan>-2-yl)-amino>propyl>amino>-1-phenylethyl>carbamate (144876-81-3)

Guidance literature:

With lithium hydroxide; In tetrahydrofuran; water; at 25 ℃;

DOI:10.1016/S0040-4020(01)86596-0

Reference yield:

2-amino-2-adamantanecarboxylic acid (42381-05-5) → phenylmethyl -<2-<<3-(1H-indol-3-yl)-2-methyl-2-<(5-oxo-spiro3,5>octan>-2-yl)-amino>propyl>amino>-1-phenylethyl>carbamate (144876-81-3)

Guidance literature:

Multi-step reaction with 6 steps

1: 16 percent / NaOH / H₂O; dioxane

2: 82 percent / diethyl ether; tetrahydrofuran / 1 h / 25 °C

3: 93 percent / H₂ / 20percent Pd-(OH)2/C / propan-2-ol / 24 h / 60 °C / 3102.9 Torr

4: 98 percent / NEt₃ / tetrahydrofuran / 4 h / 25 °C

5: 92 percent / toluene; tetrahydrofuran / 16 h / 80 - 100 °C

6: 95 percent / LiOH*H₂O / tetrahydrofuran; H₂O / 25 °C

With lithium hydroxide; sodium hydroxide; hydrogen; triethylamine; palladium hydroxide - carbon; In tetrahydrofuran; 1,4-dioxane; diethyl ether; water; isopropyl alcohol; toluene;

DOI:10.1016/S0040-4020(01)86596-0

Reference yield:

2-N-benzyloxycarbonylamino-2-hydroxycarbonyl-adamantane (144876-66-4) → phenylmethyl -<2-<<3-(1H-indol-3-yl)-2-methyl-2-<(5-oxo-spiro3,5>octan>-2-yl)-amino>propyl>amino>-1-phenylethyl>carbamate (144876-81-3)

Guidance literature:

Multi-step reaction with 5 steps

1: 82 percent / diethyl ether; tetrahydrofuran / 1 h / 25 °C

2: 93 percent / H₂ / 20percent Pd-(OH)2/C / propan-2-ol / 24 h / 60 °C / 3102.9 Torr

3: 98 percent / NEt₃ / tetrahydrofuran / 4 h / 25 °C

4: 92 percent / toluene; tetrahydrofuran / 16 h / 80 - 100 °C

5: 95 percent / LiOH*H₂O / tetrahydrofuran; H₂O / 25 °C

With lithium hydroxide; hydrogen; triethylamine; palladium hydroxide - carbon; In tetrahydrofuran; diethyl ether; water; isopropyl alcohol; toluene;

DOI:10.1016/S0040-4020(01)86596-0

upstream raw materials:

phenylmethyl-4-(1H-indol-3-ylmethyl)-1-<2-(methoxycarbonyl)tricyclo<3.3.1.1^3,7>-dec-2-yl>-4-methyl-2,5-dioxo-8-phenyl-1,3,6,9-tetraazadecan-10-oate

2-amino-2-adamantanecarboxylic acid

((S)-2-Amino-1-phenyl-ethyl)-carbamic acid benzyl ester

2-aminoadamantyl-2-carboxylic acid methyl ester