5-[1-Benzenesulfonyl-2-(1-hydroxy-prop-2-ynyl)-1H-indol-3-yl]-3-(2-trimethylsilanyl-ethoxymethyl)-3H-oxazol-2-one

Base Information

Chemical Name:5-[1-Benzenesulfonyl-2-(1-hydroxy-prop-2-ynyl)-1H-indol-3-yl]-3-(2-trimethylsilanyl-ethoxymethyl)-3H-oxazol-2-one
CAS No.:183552-13-8
Molecular Formula:C₂₆H₂₈N₂O₆SSi
Molecular Weight:524.67
Hs Code.:

Synonyms:5-[1-Benzenesulfonyl-2-(1-hydroxy-prop-2-ynyl)-1H-indol-3-yl]-3-(2-trimethylsilanyl-ethoxymethyl)-3H-oxazol-2-one

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Chemical Property of 5-[1-Benzenesulfonyl-2-(1-hydroxy-prop-2-ynyl)-1H-indol-3-yl]-3-(2-trimethylsilanyl-ethoxymethyl)-3H-oxazol-2-one

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Technology Process of 5-[1-Benzenesulfonyl-2-(1-hydroxy-prop-2-ynyl)-1H-indol-3-yl]-3-(2-trimethylsilanyl-ethoxymethyl)-3H-oxazol-2-one

There total 5 articles about 5-[1-Benzenesulfonyl-2-(1-hydroxy-prop-2-ynyl)-1H-indol-3-yl]-3-(2-trimethylsilanyl-ethoxymethyl)-3H-oxazol-2-one 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: 93.0%

: 183552-11-6
1-Benzenesulfonyl-3-[2-oxo-3-(2-trimethylsilanyl-ethoxymethyl)-2,3-dihydro-oxazol-5-yl]-1H-indole-2-carbaldehyde

: 4301-14-8
acetylenemagnesium bromide

: 183552-13-8
5-[1-Benzenesulfonyl-2-(1-hydroxy-prop-2-ynyl)-1H-indol-3-yl]-3-(2-trimethylsilanyl-ethoxymethyl)-3H-oxazol-2-one

Guidance literature:: In tetrahydrofuran;
DOI:10.3987/com-96-7532

Reference yield:

: 76513-69-4
(2-trimethylethylsilylethoxy)methyl chloride

: 183552-13-8
5-[1-Benzenesulfonyl-2-(1-hydroxy-prop-2-ynyl)-1H-indol-3-yl]-3-(2-trimethylsilanyl-ethoxymethyl)-3H-oxazol-2-one

Guidance literature:: Multi-step reaction with 4 steps

1: NaH / dimethylformamide

2: 1.) t-BuLi, n-Bu₃SnCl; 2.) Pd(PPh₃)4 / 1.) THF, -78 deg C; 2.) 100 deg C, 4 h, DMF

3: 46 percent / NaH / dimethylformamide

4: 93 percent / tetrahydrofuran

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; tributyltin chloride; tert.-butyl lithium; sodium hydride; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.3987/com-96-7532

Reference yield:

: 176327-44-9
3-iodo-1H-indole-2-carboxaldehyde

: 183552-13-8
5-[1-Benzenesulfonyl-2-(1-hydroxy-prop-2-ynyl)-1H-indol-3-yl]-3-(2-trimethylsilanyl-ethoxymethyl)-3H-oxazol-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) t-BuLi, n-Bu₃SnCl; 2.) Pd(PPh₃)4 / 1.) THF, -78 deg C; 2.) 100 deg C, 4 h, DMF

2: 46 percent / NaH / dimethylformamide

3: 93 percent / tetrahydrofuran

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; tributyltin chloride; tert.-butyl lithium; sodium hydride; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.3987/com-96-7532