1,1-dimethylethyl {3-[4-(4-morpholinylmethyl)-6-([1,3]thiazolo[5,4-b]pyridin-2-ylamino)-2-pyrimidinyl]phenyl}carbamate

Base Information

Chemical Name:1,1-dimethylethyl {3-[4-(4-morpholinylmethyl)-6-([1,3]thiazolo[5,4-b]pyridin-2-ylamino)-2-pyrimidinyl]phenyl}carbamate
CAS No.:1365838-97-6
Molecular Formula:C₂₆H₂₉N₇O₃S
Molecular Weight:519.627
Hs Code.:

Synonyms:1,1-dimethylethyl {3-[4-(4-morpholinylmethyl)-6-([1,3]thiazolo[5,4-b]pyridin-2-ylamino)-2-pyrimidinyl]phenyl}carbamate

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Chemical Property of 1,1-dimethylethyl {3-[4-(4-morpholinylmethyl)-6-([1,3]thiazolo[5,4-b]pyridin-2-ylamino)-2-pyrimidinyl]phenyl}carbamate

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Technology Process of 1,1-dimethylethyl {3-[4-(4-morpholinylmethyl)-6-([1,3]thiazolo[5,4-b]pyridin-2-ylamino)-2-pyrimidinyl]phenyl}carbamate

There total 6 articles about 1,1-dimethylethyl {3-[4-(4-morpholinylmethyl)-6-([1,3]thiazolo[5,4-b]pyridin-2-ylamino)-2-pyrimidinyl]phenyl}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: 7.0%

: 1365838-68-1
N-[2-chloro-6-(4-morpholinylmethyl)-4-pyrimidinyl][1,3]thiazolo[5,4-b]pyridin-2-amine

: 380430-68-2
3-(tert-butoxycarbonylamino)phenylboronic acid

: 1365838-97-6
1,1-dimethylethyl {3-[4-(4-morpholinylmethyl)-6-([1,3]thiazolo[5,4-b]pyridin-2-ylamino)-2-pyrimidinyl]phenyl}carbamate

Guidance literature:: With potassium phosphate; chloro(di-2-norbornylphosphino)(2'-dimethylamino-1,1'-biphenyl-2-yl)palladium(II); In 1,4-dioxane; water; at 160 ℃; for 1.5h; Microwave irradiation;

Reference yield:

: 1365838-64-7
methyl 2-chloro-6-((2,4,4-trimethylpentan-2-yl)amino)pyrimidine-4-carboxylate

: 1365838-97-6
1,1-dimethylethyl {3-[4-(4-morpholinylmethyl)-6-([1,3]thiazolo[5,4-b]pyridin-2-ylamino)-2-pyrimidinyl]phenyl}carbamate

Guidance literature:: Multi-step reaction with 5 steps

1.1: 1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]pyrimidine / tetrahydrofuran / 3 h / 20 °C

2.1: borane-THF / tetrahydrofuran / 0 - 50 °C / Inert atmosphere

2.2: 20 °C / Inert atmosphere

2.3: pH 14

3.1: trifluoroacetic acid / dichloromethane / 20 - 40 °C

4.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 2.08 h / 20 °C / Cooling

5.1: potassium phosphate / chloro(di-2-norbornylphosphino)(2'-dimethylamino-1,1'-biphenyl-2-yl)palladium(II) / 1,4-dioxane; water / 1.5 h / 160 °C / Microwave irradiation

With potassium phosphate; borane-THF; 1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]pyrimidine; sodium hydride; trifluoroacetic acid; chloro(di-2-norbornylphosphino)(2'-dimethylamino-1,1'-biphenyl-2-yl)palladium(II); In tetrahydrofuran; 1,4-dioxane; dichloromethane; water; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 1365838-65-8
2-chloro-6-(4-morpholinylcarbonyl)-N-(1,1,3,3-tetramethylbutyl)-4-pyrimidinamine

: 1365838-97-6
1,1-dimethylethyl {3-[4-(4-morpholinylmethyl)-6-([1,3]thiazolo[5,4-b]pyridin-2-ylamino)-2-pyrimidinyl]phenyl}carbamate

Guidance literature:: Multi-step reaction with 4 steps

1.1: borane-THF / tetrahydrofuran / 0 - 50 °C / Inert atmosphere

1.2: 20 °C / Inert atmosphere

1.3: pH 14

2.1: trifluoroacetic acid / dichloromethane / 20 - 40 °C

3.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 2.08 h / 20 °C / Cooling

4.1: potassium phosphate / chloro(di-2-norbornylphosphino)(2'-dimethylamino-1,1'-biphenyl-2-yl)palladium(II) / 1,4-dioxane; water / 1.5 h / 160 °C / Microwave irradiation

With potassium phosphate; borane-THF; sodium hydride; trifluoroacetic acid; chloro(di-2-norbornylphosphino)(2'-dimethylamino-1,1'-biphenyl-2-yl)palladium(II); In tetrahydrofuran; 1,4-dioxane; dichloromethane; water; N,N-dimethyl-formamide; mineral oil;