[4-(tert-butyldimethylsilanyloxymethyl)pyridin-2-yl](5-phenylthiazol-2-yl)amine

Base Information

Chemical Name:[4-(tert-butyldimethylsilanyloxymethyl)pyridin-2-yl](5-phenylthiazol-2-yl)amine
CAS No.:329794-10-7
Molecular Formula:C₂₁H₂₇N₃OSSi
Molecular Weight:397.616
Hs Code.:

Synonyms:[4-(tert-butyldimethylsilanyloxymethyl)pyridin-2-yl](5-phenylthiazol-2-yl)amine

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Chemical Property of [4-(tert-butyldimethylsilanyloxymethyl)pyridin-2-yl](5-phenylthiazol-2-yl)amine

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Technology Process of [4-(tert-butyldimethylsilanyloxymethyl)pyridin-2-yl](5-phenylthiazol-2-yl)amine

There total 5 articles about [4-(tert-butyldimethylsilanyloxymethyl)pyridin-2-yl](5-phenylthiazol-2-yl)amine 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: 79.0%

: 329794-40-3
2-chloro-5-phenyl-thiazole

: 329794-09-4
4-({[tert-butyl(dimethyl)silyl]oxy}methyl)pyridin-2-amine

: 329794-10-7
[4-(tert-butyldimethylsilanyloxymethyl)pyridin-2-yl](5-phenylthiazol-2-yl)amine

Guidance literature:: 4-({[tert-butyl(dimethyl)silyl]oxy}methyl)pyridin-2-amine; With sodium hydride; In tetrahydrofuran; at 20 ℃;

2-chloro-5-phenyl-thiazole; In tetrahydrofuran; for 2h; Heating;
DOI:10.1021/jm049697f

Reference yield:

: 100704-10-7
(2-chloropyridin-4-yl)methanol

: 329794-10-7
[4-(tert-butyldimethylsilanyloxymethyl)pyridin-2-yl](5-phenylthiazol-2-yl)amine

Guidance literature:: Multi-step reaction with 4 steps

1.1: 97 percent / imidazole / tetrahydrofuran / 24 h / 20 °C

2.1: NaOtBu; BINAP racemic; Pd₂(dba)3 / toluene / 5 h / 80 °C

3.1: 17.89 g / aq. hydroxylamine / methanol / 18 h / 20 °C

4.1: NaH / tetrahydrofuran / 20 °C

4.2: 79 percent / tetrahydrofuran / 2 h / Heating

With 1H-imidazole; tris(dibenzylideneacetone)dipalladium ⁽⁰⁾; hydroxylamine; sodium hydride; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate; In tetrahydrofuran; methanol; toluene;
DOI:10.1021/jm049697f

Reference yield:

: 18162-48-6
tert-butyldimethylsilyl chloride

: 329794-10-7
[4-(tert-butyldimethylsilanyloxymethyl)pyridin-2-yl](5-phenylthiazol-2-yl)amine

Guidance literature:: Multi-step reaction with 4 steps

1.1: 97 percent / imidazole / tetrahydrofuran / 24 h / 20 °C

2.1: NaOtBu; BINAP racemic; Pd₂(dba)3 / toluene / 5 h / 80 °C

3.1: 17.89 g / aq. hydroxylamine / methanol / 18 h / 20 °C

4.1: NaH / tetrahydrofuran / 20 °C

4.2: 79 percent / tetrahydrofuran / 2 h / Heating

With 1H-imidazole; tris(dibenzylideneacetone)dipalladium ⁽⁰⁾; hydroxylamine; sodium hydride; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate; In tetrahydrofuran; methanol; toluene;
DOI:10.1021/jm049697f