tert-butyl (1-(4-(9H-benzo[f]pyrido[2,3-b][1,2,4]triazolo[4,3-d][1,4]diazepin-3-yl)benzyl)piperidin-4-yl)carbamate

Base Information

Chemical Name:tert-butyl (1-(4-(9H-benzo[f]pyrido[2,3-b][1,2,4]triazolo[4,3-d][1,4]diazepin-3-yl)benzyl)piperidin-4-yl)carbamate
CAS No.:1338243-36-9
Molecular Formula:C₃₀H₃₃N₇O₂
Molecular Weight:523.638
Hs Code.:

Synonyms:tert-butyl (1-(4-(9H-benzo[f]pyrido[2,3-b][1,2,4]triazolo[4,3-d][1,4]diazepin-3-yl)benzyl)piperidin-4-yl)carbamate

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Chemical Property of tert-butyl (1-(4-(9H-benzo[f]pyrido[2,3-b][1,2,4]triazolo[4,3-d][1,4]diazepin-3-yl)benzyl)piperidin-4-yl)carbamate

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Technology Process of tert-butyl (1-(4-(9H-benzo[f]pyrido[2,3-b][1,2,4]triazolo[4,3-d][1,4]diazepin-3-yl)benzyl)piperidin-4-yl)carbamate

There total 6 articles about tert-butyl (1-(4-(9H-benzo[f]pyrido[2,3-b][1,2,4]triazolo[4,3-d][1,4]diazepin-3-yl)benzyl)piperidin-4-yl)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: 69.0%

: 1338242-45-7
3-(4-(chloromethyl)phenyl)-9H-benzo[f]pyrido[2,3-b][1,2,4]triazolo[4,3-d][1,4]diazepine

: 73874-95-0
(piperidin-4-yl)carbamic acid tert-butyl ester

: 1338243-36-9
tert-butyl (1-(4-(9H-benzo[f]pyrido[2,3-b][1,2,4]triazolo[4,3-d][1,4]diazepin-3-yl)benzyl)piperidin-4-yl)carbamate

Guidance literature:: With triethylamine; In ISOPROPYLAMIDE; at 75 ℃; for 20h;

Reference yield:

: 6908-41-4,58590-49-1
4-(methoxycarbonyl)benzyl alcohol

: 1338243-36-9
tert-butyl (1-(4-(9H-benzo[f]pyrido[2,3-b][1,2,4]triazolo[4,3-d][1,4]diazepin-3-yl)benzyl)piperidin-4-yl)carbamate

Guidance literature:: Multi-step reaction with 4 steps

1: hydrazine hydrate / ethanol / 20 h / Reflux

2: triethylamine / ISOPROPYLAMIDE / 85 °C

3: thionyl chloride / dichloromethane / 1 h / 20 °C

4: triethylamine / ISOPROPYLAMIDE / 20 h / 75 °C

With thionyl chloride; hydrazine hydrate; triethylamine; In ethanol; dichloromethane; ISOPROPYLAMIDE;

Reference yield:

: 58855-42-8
4-(hydroxymethyl)benzoic hydrazide

: 1338243-36-9
tert-butyl (1-(4-(9H-benzo[f]pyrido[2,3-b][1,2,4]triazolo[4,3-d][1,4]diazepin-3-yl)benzyl)piperidin-4-yl)carbamate

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / ISOPROPYLAMIDE / 85 °C

2: thionyl chloride / dichloromethane / 1 h / 20 °C

3: triethylamine / ISOPROPYLAMIDE / 20 h / 75 °C

With thionyl chloride; triethylamine; In dichloromethane; ISOPROPYLAMIDE;