2-(4-{[(1S,3R,5S)-3,5-Bis-(trityl-amino)-cyclohexyl]-pyridin-2-ylmethyl-amino}-butyl)-isoindole-1,3-dione

Base Information

Chemical Name:2-(4-{[(1S,3R,5S)-3,5-Bis-(trityl-amino)-cyclohexyl]-pyridin-2-ylmethyl-amino}-butyl)-isoindole-1,3-dione
CAS No.:479251-93-9
Molecular Formula:C₆₂H₅₉N₅O₂
Molecular Weight:906.183
Hs Code.:

Synonyms:2-(4-{[(1S,3R,5S)-3,5-Bis-(trityl-amino)-cyclohexyl]-pyridin-2-ylmethyl-amino}-butyl)-isoindole-1,3-dione

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2-(4-{[(1S,3R,5S)-3,5-Bis-(trityl-amino)-cyclohexyl]-pyridin-2-ylmethyl-amino}-butyl)-isoindole-1,3-dione

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of 2-(4-{[(1S,3R,5S)-3,5-Bis-(trityl-amino)-cyclohexyl]-pyridin-2-ylmethyl-amino}-butyl)-isoindole-1,3-dione

There total 5 articles about 2-(4-{[(1S,3R,5S)-3,5-Bis-(trityl-amino)-cyclohexyl]-pyridin-2-ylmethyl-amino}-butyl)-isoindole-1,3-dione 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: 81.0%

: 5394-18-3
2-(4-bromobutyl)isoindoline-1,3-dione

: 479251-89-3
N-(2-pyridylmethyl)-N',N''-bis-trityl-cis,cis-1,3,5-triaminocyclohexane

: 479251-93-9
2-(4-{[(1S,3R,5S)-3,5-Bis-(trityl-amino)-cyclohexyl]-pyridin-2-ylmethyl-amino}-butyl)-isoindole-1,3-dione

Guidance literature:: With potassium carbonate; In acetonitrile; for 36h; Heating;
DOI:10.1021/jo0204911

Reference yield:

: 1121-60-4
pyridine-2-carbaldehyde

: 479251-93-9
2-(4-{[(1S,3R,5S)-3,5-Bis-(trityl-amino)-cyclohexyl]-pyridin-2-ylmethyl-amino}-butyl)-isoindole-1,3-dione

Guidance literature:: Multi-step reaction with 3 steps

1: benzene / 7 h / Heating

2: 656 mg / NaBH₄ / ethanol / 24 h / 20 °C

3: 81 percent / K₂CO₃ / acetonitrile / 36 h / Heating

With sodium tetrahydroborate; potassium carbonate; In ethanol; acetonitrile; benzene;
DOI:10.1021/jo0204911

Reference yield:

: 76-83-5
trityl chloride

: 479251-93-9
2-(4-{[(1S,3R,5S)-3,5-Bis-(trityl-amino)-cyclohexyl]-pyridin-2-ylmethyl-amino}-butyl)-isoindole-1,3-dione

Guidance literature:: Multi-step reaction with 4 steps

1: 52 percent / CHCl₃ / 2 h / Heating

2: benzene / 7 h / Heating

3: 656 mg / NaBH₄ / ethanol / 24 h / 20 °C

4: 81 percent / K₂CO₃ / acetonitrile / 36 h / Heating

With sodium tetrahydroborate; potassium carbonate; In ethanol; chloroform; acetonitrile; benzene;
DOI:10.1021/jo0204911