benzyl {(1R,2R,5S)-2-(cyanomethyl)-5[(6-nitrothieno[3,2-b]pyridin-7-yl)amino]cyclohexyl}carbamate

Base Information

Chemical Name:benzyl {(1R,2R,5S)-2-(cyanomethyl)-5[(6-nitrothieno[3,2-b]pyridin-7-yl)amino]cyclohexyl}carbamate
CAS No.:1607592-07-3
Molecular Formula:C₂₃H₂₃N₅O₄S
Molecular Weight:465.533
Hs Code.:

Synonyms:benzyl {(1R,2R,5S)-2-(cyanomethyl)-5[(6-nitrothieno[3,2-b]pyridin-7-yl)amino]cyclohexyl}carbamate

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Chemical Property of benzyl {(1R,2R,5S)-2-(cyanomethyl)-5[(6-nitrothieno[3,2-b]pyridin-7-yl)amino]cyclohexyl}carbamate

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Technology Process of benzyl {(1R,2R,5S)-2-(cyanomethyl)-5[(6-nitrothieno[3,2-b]pyridin-7-yl)amino]cyclohexyl}carbamate

There total 4 articles about benzyl {(1R,2R,5S)-2-(cyanomethyl)-5[(6-nitrothieno[3,2-b]pyridin-7-yl)amino]cyclohexyl}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:

: 69627-02-7,107818-20-2
thieno[3,2-b]pyridin-7-ol

: 1607592-07-3
benzyl {(1R,2R,5S)-2-(cyanomethyl)-5[(6-nitrothieno[3,2-b]pyridin-7-yl)amino]cyclohexyl}carbamate

Guidance literature:: Multi-step reaction with 3 steps

1.1: tetrabutylammonium nitrate / dichloromethane / -5 °C

1.2: -5 - 20 °C

2.1: trichlorophosphate / 1 h / Reflux

3.1: triethylamine / isopropyl alcohol / 2 h / 90 °C

With tetrabutylammonium nitrate; triethylamine; trichlorophosphate; In dichloromethane; isopropyl alcohol;

Reference yield:

: 110651-92-8
7-chloro-6-nitrothieno[3,2-b]pyridine

: 1607592-06-2
benzyl [(1R,2R,5S)-5-amino-2-(cyanomethyl)cyclohexyl]carbamate

: 1607592-07-3
benzyl {(1R,2R,5S)-2-(cyanomethyl)-5[(6-nitrothieno[3,2-b]pyridin-7-yl)amino]cyclohexyl}carbamate

Guidance literature:: With triethylamine; In isopropyl alcohol; at 90 ℃; for 2h;

Reference yield:

: benzyl [(1R,2R,5S)-5-azido-2-(cyanomethyl)cyclohexyl]carbamate

: 1607592-07-3
benzyl {(1R,2R,5S)-2-(cyanomethyl)-5[(6-nitrothieno[3,2-b]pyridin-7-yl)amino]cyclohexyl}carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: triphenylphosphine / water; tetrahydrofuran / 20 °C

2: triethylamine / isopropyl alcohol / 2 h / 90 °C

With triethylamine; triphenylphosphine; In tetrahydrofuran; water; isopropyl alcohol;