[[(S)-(1H-Indol-4-yl)-((S)-2,2,5,5-tetramethyl-[1,3]dioxolan-4-yl)-methyl]-(toluene-4-sulfonyl)-amino]-acetic acid methyl ester

Base Information

Chemical Name:[[(S)-(1H-Indol-4-yl)-((S)-2,2,5,5-tetramethyl-[1,3]dioxolan-4-yl)-methyl]-(toluene-4-sulfonyl)-amino]-acetic acid methyl ester
CAS No.:88299-10-9
Molecular Formula:C₂₆H₃₂N₂O₆S
Molecular Weight:500.616
Hs Code.:

Synonyms:[[(S)-(1H-Indol-4-yl)-((S)-2,2,5,5-tetramethyl-[1,3]dioxolan-4-yl)-methyl]-(toluene-4-sulfonyl)-amino]-acetic acid methyl ester

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Chemical Property of [[(S)-(1H-Indol-4-yl)-((S)-2,2,5,5-tetramethyl-[1,3]dioxolan-4-yl)-methyl]-(toluene-4-sulfonyl)-amino]-acetic acid methyl ester

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Technology Process of [[(S)-(1H-Indol-4-yl)-((S)-2,2,5,5-tetramethyl-[1,3]dioxolan-4-yl)-methyl]-(toluene-4-sulfonyl)-amino]-acetic acid methyl ester

There total 9 articles about [[(S)-(1H-Indol-4-yl)-((S)-2,2,5,5-tetramethyl-[1,3]dioxolan-4-yl)-methyl]-(toluene-4-sulfonyl)-amino]-acetic acid methyl 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: 70.0%

: 186581-53-3,908094-01-9,334-88-3
diazomethane

: [[(S)-(1H-Indol-4-yl)-((S)-2,2,5,5-tetramethyl-[1,3]dioxolan-4-yl)-methyl]-(toluene-4-sulfonyl)-amino]-acetic acid

: 88299-10-9
[[(S)-(1H-Indol-4-yl)-((S)-2,2,5,5-tetramethyl-[1,3]dioxolan-4-yl)-methyl]-(toluene-4-sulfonyl)-amino]-acetic acid methyl ester

Guidance literature:: In methanol; diethyl ether;

Reference yield:

: 88299-06-3
(E)-2-methyl-4-(1-tosyl-1H-indol-4-yl)but-3-en-2-ol

: 88299-10-9
[[(S)-(1H-Indol-4-yl)-((S)-2,2,5,5-tetramethyl-[1,3]dioxolan-4-yl)-methyl]-(toluene-4-sulfonyl)-amino]-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 1.) m-ClC₆H₄CO₃H, 2.) NaN₃ / 1.) CH₂Cl₂, from 0 deg C to rt, 2.) dioxane, water, reflux

2: 93 percent / p-TsOH / Ambient temperature

3: H₂ / PtO₂ / methanol / Ambient temperature

4: Et₃N / 1,2-dichloro-ethane / Heating

5: K₂CO₃ / dimethylformamide / Ambient temperature

6: 20percent KOH / methanol; 1,2-dimethoxy-ethane; H₂O

7: 70 percent / methanol; diethyl ether

With potassium hydroxide; sodium azide; hydrogen; potassium carbonate; triethylamine; 3-chloro-benzenecarboperoxoic acid; platinum(IV) oxide; toluene-4-sulfonic acid; In methanol; 1,2-dimethoxyethane; diethyl ether; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide;

Reference yield:

: 88246-05-3
(E)-4-(1-tosyl-1H-indol-4-yl)but-3-en-2-one

: 88299-10-9
[[(S)-(1H-Indol-4-yl)-((S)-2,2,5,5-tetramethyl-[1,3]dioxolan-4-yl)-methyl]-(toluene-4-sulfonyl)-amino]-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 8 steps

1: 70 percent / diethyl ether; tetrahydrofuran / 0 °C

2: 1.) m-ClC₆H₄CO₃H, 2.) NaN₃ / 1.) CH₂Cl₂, from 0 deg C to rt, 2.) dioxane, water, reflux

3: 93 percent / p-TsOH / Ambient temperature

4: H₂ / PtO₂ / methanol / Ambient temperature

5: Et₃N / 1,2-dichloro-ethane / Heating

6: K₂CO₃ / dimethylformamide / Ambient temperature

7: 20percent KOH / methanol; 1,2-dimethoxy-ethane; H₂O

8: 70 percent / methanol; diethyl ether

With potassium hydroxide; sodium azide; hydrogen; potassium carbonate; triethylamine; 3-chloro-benzenecarboperoxoic acid; platinum(IV) oxide; toluene-4-sulfonic acid; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; diethyl ether; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide;