1,1-dimethylethyl (2,3-dihydro[1,4]dioxino[2,3-c]pyridin-7-ylmethyl){6-[(diphenylmethylidene)amino]-1,2,3,4-tetrahydro-2-naphthalenyl}carbamate

Base Information

Chemical Name:1,1-dimethylethyl (2,3-dihydro[1,4]dioxino[2,3-c]pyridin-7-ylmethyl){6-[(diphenylmethylidene)amino]-1,2,3,4-tetrahydro-2-naphthalenyl}carbamate
CAS No.:1073632-76-4
Molecular Formula:C₃₆H₃₇N₃O₄
Molecular Weight:575.707
Hs Code.:

1,1-dimethylethyl (2,3-dihydro[1,4]dioxino[2,3-c]pyridin-7-ylmethyl){6-[(diphenylmethylidene)amino]-1,2,3,4-tetrahydro-2-naphthalenyl}carbamate

Synonyms:1,1-dimethylethyl (2,3-dihydro[1,4]dioxino[2,3-c]pyridin-7-ylmethyl){6-[(diphenylmethylidene)amino]-1,2,3,4-tetrahydro-2-naphthalenyl}carbamate

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Chemical Property of 1,1-dimethylethyl (2,3-dihydro[1,4]dioxino[2,3-c]pyridin-7-ylmethyl){6-[(diphenylmethylidene)amino]-1,2,3,4-tetrahydro-2-naphthalenyl}carbamate

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Technology Process of 1,1-dimethylethyl (2,3-dihydro[1,4]dioxino[2,3-c]pyridin-7-ylmethyl){6-[(diphenylmethylidene)amino]-1,2,3,4-tetrahydro-2-naphthalenyl}carbamate

There total 6 articles about 1,1-dimethylethyl (2,3-dihydro[1,4]dioxino[2,3-c]pyridin-7-ylmethyl){6-[(diphenylmethylidene)amino]-1,2,3,4-tetrahydro-2-naphthalenyl}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: 99.0%

: 1013-88-3
Benzophenone imine

: 1,1-dimethyl ethyl (6-bromo-1,2,3,4-tetrahydro-2-naphthalenyl)(2,3-dihydro[1,4]dioxino[2,3-c]pyridin-7-ylmethyl)carbamate

: 1073632-76-4
1,1-dimethylethyl (2,3-dihydro[1,4]dioxino[2,3-c]pyridin-7-ylmethyl){6-[(diphenylmethylidene)amino]-1,2,3,4-tetrahydro-2-naphthalenyl}carbamate

Guidance literature:: With sodium t-butanolate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; In toluene; at 20 - 100 ℃;

Reference yield:

: 917836-01-2
(2,3-dihydro-[1,4]dioxino[2,3-c]pyridin-7-yl)methanamine

: 1073632-76-4
1,1-dimethylethyl (2,3-dihydro[1,4]dioxino[2,3-c]pyridin-7-ylmethyl){6-[(diphenylmethylidene)amino]-1,2,3,4-tetrahydro-2-naphthalenyl}carbamate

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium tris(acetoxy)borohydride / methanol; chloroform / 16 h / 20 °C

2.1: sodium hydrogencarbonate / methanol / 0.17 h / 20 °C

2.2: 0 - 20 °C

3.1: sodium t-butanolate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl / toluene / 20 - 100 °C

With sodium tris(acetoxy)borohydride; sodium hydrogencarbonate; sodium t-butanolate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; In methanol; chloroform; toluene;

Reference yield:

: 1073632-73-1
(6-bromo-1,2,3,4-tetrahydro-2-naphthalenyl)(2,3-dihydro[1,4]dioxino[2,3-c]pyridin-7-ylmethyl)amine

: 1073632-76-4
1,1-dimethylethyl (2,3-dihydro[1,4]dioxino[2,3-c]pyridin-7-ylmethyl){6-[(diphenylmethylidene)amino]-1,2,3,4-tetrahydro-2-naphthalenyl}carbamate

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydrogencarbonate / methanol / 0.17 h / 20 °C

1.2: 0 - 20 °C

2.1: sodium t-butanolate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl / toluene / 20 - 100 °C

With sodium hydrogencarbonate; sodium t-butanolate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; In methanol; toluene;