3-[3-(R)-(tert-butyldimethylsilanyloxymethyl)-1-(4-methoxybenzenesulfonyl)aziridin-2-(S)-ylmethoxy]pyridine

Base Information

Chemical Name:3-[3-(R)-(tert-butyldimethylsilanyloxymethyl)-1-(4-methoxybenzenesulfonyl)aziridin-2-(S)-ylmethoxy]pyridine
CAS No.:370064-99-6
Molecular Formula:C₂₂H₃₂N₂O₅SSi
Molecular Weight:464.658
Hs Code.:

Synonyms:3-[3-(R)-(tert-butyldimethylsilanyloxymethyl)-1-(4-methoxybenzenesulfonyl)aziridin-2-(S)-ylmethoxy]pyridine

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Chemical Property of 3-[3-(R)-(tert-butyldimethylsilanyloxymethyl)-1-(4-methoxybenzenesulfonyl)aziridin-2-(S)-ylmethoxy]pyridine

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Technology Process of 3-[3-(R)-(tert-butyldimethylsilanyloxymethyl)-1-(4-methoxybenzenesulfonyl)aziridin-2-(S)-ylmethoxy]pyridine

There total 4 articles about 3-[3-(R)-(tert-butyldimethylsilanyloxymethyl)-1-(4-methoxybenzenesulfonyl)aziridin-2-(S)-ylmethoxy]pyridine 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: 97.0%

: 98-68-0
4-methoxy-phenyl-sulphonyl chloride

: 370064-98-5
3-[3-(R)-(tert-butyldimethylsilanyloxymethyl)aziridin-2-(S)-ylmethoxy]pyridine

: 370064-99-6
3-[3-(R)-(tert-butyldimethylsilanyloxymethyl)-1-(4-methoxybenzenesulfonyl)aziridin-2-(S)-ylmethoxy]pyridine

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃; for 12h;
DOI:10.1016/S0040-4020(01)00641-X

Reference yield:

: 370064-96-3
[1-benzyloxy-3-(S)-(pyridin-3-yloxymethyl)aziridine-2-(R)-yl]methanol

: 370064-99-6
3-[3-(R)-(tert-butyldimethylsilanyloxymethyl)-1-(4-methoxybenzenesulfonyl)aziridin-2-(S)-ylmethoxy]pyridine

Guidance literature:: Multi-step reaction with 3 steps

1: 87 percent / 2,6-lutidine / CH₂Cl₂ / 0.5 h / 0 °C

2: 97 percent / H₂ / Pd/BaSO₄ / ethanol / 14 h / 760 Torr

3: 97 percent / Et₃N / CH₂Cl₂ / 12 h / 0 °C

With 2,6-dimethylpyridine; hydrogen; triethylamine; Pd-BaSO₄; In ethanol; dichloromethane;
DOI:10.1016/S0040-4020(01)00641-X

Reference yield:

: 370064-95-2
1-benzyloxy-3-(S)-(pyridin-3-yloxymethyl)aziridine-2-(R)-carboxylic acid tert-butyl ester

: 370064-99-6
3-[3-(R)-(tert-butyldimethylsilanyloxymethyl)-1-(4-methoxybenzenesulfonyl)aziridin-2-(S)-ylmethoxy]pyridine

Guidance literature:: Multi-step reaction with 4 steps

1: 77 percent / DIBALH / CH₂Cl₂; toluene / 1 h / -78 - 0 °C

2: 87 percent / 2,6-lutidine / CH₂Cl₂ / 0.5 h / 0 °C

3: 97 percent / H₂ / Pd/BaSO₄ / ethanol / 14 h / 760 Torr

4: 97 percent / Et₃N / CH₂Cl₂ / 12 h / 0 °C

With 2,6-dimethylpyridine; hydrogen; diisobutylaluminium hydride; triethylamine; Pd-BaSO₄; In ethanol; dichloromethane; toluene;
DOI:10.1016/S0040-4020(01)00641-X