tert-butyl [2,6-dimethyl-4-(5-methylsulfanyl-7-propyloxazolo[5,4-d]pyrimidin-2-yl)phenoxy]acetate

Base Information

Chemical Name:tert-butyl [2,6-dimethyl-4-(5-methylsulfanyl-7-propyloxazolo[5,4-d]pyrimidin-2-yl)phenoxy]acetate
CAS No.:1417620-30-4
Molecular Formula:C₂₃H₂₉N₃O₄S
Molecular Weight:443.567
Hs Code.:

Synonyms:tert-butyl [2,6-dimethyl-4-(5-methylsulfanyl-7-propyloxazolo[5,4-d]pyrimidin-2-yl)phenoxy]acetate

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Chemical Property of tert-butyl [2,6-dimethyl-4-(5-methylsulfanyl-7-propyloxazolo[5,4-d]pyrimidin-2-yl)phenoxy]acetate

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Technology Process of tert-butyl [2,6-dimethyl-4-(5-methylsulfanyl-7-propyloxazolo[5,4-d]pyrimidin-2-yl)phenoxy]acetate

There total 6 articles about tert-butyl [2,6-dimethyl-4-(5-methylsulfanyl-7-propyloxazolo[5,4-d]pyrimidin-2-yl)phenoxy]acetate 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: 10.0%

: 1417620-29-1
tert-butyl [4-(7-chloro-5-methylsulfanyloxazolo[5,4-d]pyrimidin-2-yl)-2,6-dimethylphenoxy]acetate

: 927-77-5
n-propylmagnesium bromide

: 1417620-30-4
tert-butyl [2,6-dimethyl-4-(5-methylsulfanyl-7-propyloxazolo[5,4-d]pyrimidin-2-yl)phenoxy]acetate

Guidance literature:: With iron(III)-acetylacetonate; In tetrahydrofuran; at -78 - 20 ℃; for 3h; Inert atmosphere;

Reference yield:

: 1315456-71-3
sodium 4,6-dihydroxy-5-(4-methoxy-3,5-dimethyl-benzoylamino)-pyrimidine-2-thiolate

: 1417620-30-4
tert-butyl [2,6-dimethyl-4-(5-methylsulfanyl-7-propyloxazolo[5,4-d]pyrimidin-2-yl)phenoxy]acetate

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydroxide / water; 1-methyl-pyrrolidin-2-one / 0.5 h / 0 °C

1.2: 2 h / 0 °C

1.3: pH 2

2.1: trichlorophosphate / 36 h / 70 °C

3.1: boron tribromide / dichloromethane / 4 h / -20 - 20 °C

3.2: -20 °C

4.1: potassium carbonate / N,N-dimethyl-formamide / 1 h / 60 °C

5.1: iron(III)-acetylacetonate / tetrahydrofuran / 3 h / -78 - 20 °C / Inert atmosphere

With iron(III)-acetylacetonate; boron tribromide; potassium carbonate; sodium hydroxide; trichlorophosphate; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 21668-34-8
3,5-dimethyl-4-methoxybenzoic acid chloride

: 1417620-30-4
tert-butyl [2,6-dimethyl-4-(5-methylsulfanyl-7-propyloxazolo[5,4-d]pyrimidin-2-yl)phenoxy]acetate

Guidance literature:: Multi-step reaction with 7 steps

1.1: triethylamine / dichloromethane / 2 h / 0 °C

2.1: sodium methylate / ethanol; methanol / 0.25 h

2.2: 3 h / 60 °C

3.1: sodium hydroxide / water; 1-methyl-pyrrolidin-2-one / 0.5 h / 0 °C

3.2: 2 h / 0 °C

3.3: pH 2

4.1: trichlorophosphate / 36 h / 70 °C

5.1: boron tribromide / dichloromethane / 4 h / -20 - 20 °C

5.2: -20 °C

6.1: potassium carbonate / N,N-dimethyl-formamide / 1 h / 60 °C

7.1: iron(III)-acetylacetonate / tetrahydrofuran / 3 h / -78 - 20 °C / Inert atmosphere

With iron(III)-acetylacetonate; sodium methylate; boron tribromide; potassium carbonate; triethylamine; sodium hydroxide; trichlorophosphate; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide;