9-(quinolin-3-yl)-2-((1-tosyl-1H-indol-3-yl)methyl)-2,9-diazaspiro[5.5]undecan-1-one

Base Information

Chemical Name:9-(quinolin-3-yl)-2-((1-tosyl-1H-indol-3-yl)methyl)-2,9-diazaspiro[5.5]undecan-1-one
CAS No.:1313237-10-3
Molecular Formula:C₃₄H₃₄N₄O₃S
Molecular Weight:578.735
Hs Code.:

Synonyms:9-(quinolin-3-yl)-2-((1-tosyl-1H-indol-3-yl)methyl)-2,9-diazaspiro[5.5]undecan-1-one

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Chemical Property of 9-(quinolin-3-yl)-2-((1-tosyl-1H-indol-3-yl)methyl)-2,9-diazaspiro[5.5]undecan-1-one

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Technology Process of 9-(quinolin-3-yl)-2-((1-tosyl-1H-indol-3-yl)methyl)-2,9-diazaspiro[5.5]undecan-1-one

There total 5 articles about 9-(quinolin-3-yl)-2-((1-tosyl-1H-indol-3-yl)methyl)-2,9-diazaspiro[5.5]undecan-1-one 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: 68.0%

: 5332-24-1
3-bromoquinoline

: 1313237-08-9
2-((1-tosyl-1H-indol-3-yl)methyl)-2,9-diazaspiro[5.5]undecan-1-one trifluoroacetate

: 1313237-10-3
9-(quinolin-3-yl)-2-((1-tosyl-1H-indol-3-yl)methyl)-2,9-diazaspiro[5.5]undecan-1-one

Guidance literature:: With sodium t-butanolate; DavePhos; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In 1,4-dioxane; at 100 ℃; for 1h; Inert atmosphere; Sealed microwave tube;

Reference yield:

: 1313236-57-5
1-tert-butyl 4-ethyl 4-(2-cyanoethyl)piperidine-1,4-dicarboxylate

: 1313237-10-3
9-(quinolin-3-yl)-2-((1-tosyl-1H-indol-3-yl)methyl)-2,9-diazaspiro[5.5]undecan-1-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogen; ammonia / Raney Ni / ethanol / 48 h / 20 °C / 5171.62 Torr / autoclave

2.1: diisopropylamine; n-butyllithium / tetrahydrofuran / 1.05 h / 0 °C

2.2: 0 - 20 °C

3.1: dichloromethane / 1.17 h / 20 °C

4.1: DavePhos; sodium t-butanolate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1,4-dioxane / 1 h / 100 °C / Inert atmosphere; Sealed microwave tube

With n-butyllithium; ammonia; hydrogen; diisopropylamine; sodium t-butanolate; DavePhos; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane;

Reference yield:

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

: 1313237-10-3
9-(quinolin-3-yl)-2-((1-tosyl-1H-indol-3-yl)methyl)-2,9-diazaspiro[5.5]undecan-1-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: diisopropylamine; n-butyllithium / tetrahydrofuran / 1.05 h / 0 °C

1.2: 0 - 20 °C

2.1: dichloromethane / 1.17 h / 20 °C

3.1: DavePhos; sodium t-butanolate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1,4-dioxane / 1 h / 100 °C / Inert atmosphere; Sealed microwave tube

With n-butyllithium; diisopropylamine; sodium t-butanolate; DavePhos; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; dichloromethane;