N'-acetyl-1-oxo-2-((1-tosyl-1H-indol-3-yl)methyl)-2,9-diazaspiro[5.5]undecane-9-carbohydrazide

Base Information

Chemical Name:N'-acetyl-1-oxo-2-((1-tosyl-1H-indol-3-yl)methyl)-2,9-diazaspiro[5.5]undecane-9-carbohydrazide
CAS No.:1373766-41-6
Molecular Formula:C₂₈H₃₃N₅O₅S
Molecular Weight:551.667
Hs Code.:

Synonyms:N'-acetyl-1-oxo-2-((1-tosyl-1H-indol-3-yl)methyl)-2,9-diazaspiro[5.5]undecane-9-carbohydrazide

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Chemical Property of N'-acetyl-1-oxo-2-((1-tosyl-1H-indol-3-yl)methyl)-2,9-diazaspiro[5.5]undecane-9-carbohydrazide

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Technology Process of N'-acetyl-1-oxo-2-((1-tosyl-1H-indol-3-yl)methyl)-2,9-diazaspiro[5.5]undecane-9-carbohydrazide

There total 3 articles about N'-acetyl-1-oxo-2-((1-tosyl-1H-indol-3-yl)methyl)-2,9-diazaspiro[5.5]undecane-9-carbohydrazide 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:

: 58550-81-5
3-(bromomethyl)-1-[(4-methylphenyl)sulfonyl]-1H-indole

: 1373766-41-6
N'-acetyl-1-oxo-2-((1-tosyl-1H-indol-3-yl)methyl)-2,9-diazaspiro[5.5]undecane-9-carbohydrazide

Guidance literature:: Multi-step reaction with 3 steps

1.1: diisopropylamine; n-butyllithium / tetrahydrofuran / 0.55 h / 0 °C

1.2: 0 - 20 °C

2.1: dichloromethane / 1.17 h / 20 °C

3.1: tetrahydrofuran / 70 h / Reflux

With n-butyllithium; diisopropylamine; In tetrahydrofuran; dichloromethane;

Reference yield:

: 1198284-94-4
tert-butyl 1-oxo-2,9-diazaspiro[5.5]undecane-9-carboxylate

: 1373766-41-6
N'-acetyl-1-oxo-2-((1-tosyl-1H-indol-3-yl)methyl)-2,9-diazaspiro[5.5]undecane-9-carbohydrazide

Guidance literature:: Multi-step reaction with 3 steps

1.1: diisopropylamine; n-butyllithium / tetrahydrofuran / 0.55 h / 0 °C

1.2: 0 - 20 °C

2.1: dichloromethane / 1.17 h / 20 °C

3.1: tetrahydrofuran / 70 h / Reflux

With n-butyllithium; diisopropylamine; In tetrahydrofuran; dichloromethane;

Reference yield:

: 1313237-05-6
tert-butyl 1-oxo-2-((1-tosyl-1H-indol-3-yl)methyl)-2,9-diazaspiro[5.5]undecane-9-carboxylate

: 1373766-41-6
N'-acetyl-1-oxo-2-((1-tosyl-1H-indol-3-yl)methyl)-2,9-diazaspiro[5.5]undecane-9-carbohydrazide

Guidance literature:: Multi-step reaction with 2 steps

1: dichloromethane / 1.17 h / 20 °C

2: tetrahydrofuran / 70 h / Reflux

In tetrahydrofuran; dichloromethane;