ethyl 2-(((2-(4-(acetamidomethyl)phenyl)-4-morpholinothieno[3,2-d]pyrimidine-6-yl)Methyl)(methyl)amino)pyrimidine-5-carboxylate

Base Information

Chemical Name:ethyl 2-(((2-(4-(acetamidomethyl)phenyl)-4-morpholinothieno[3,2-d]pyrimidine-6-yl)Methyl)(methyl)amino)pyrimidine-5-carboxylate
CAS No.:1235450-95-9
Molecular Formula:C₂₈H₃₁N₇O₄S
Molecular Weight:561.665
Hs Code.:

Synonyms:ethyl 2-(((2-(4-(acetamidomethyl)phenyl)-4-morpholinothieno[3,2-d]pyrimidine-6-yl)Methyl)(methyl)amino)pyrimidine-5-carboxylate

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Chemical Property of ethyl 2-(((2-(4-(acetamidomethyl)phenyl)-4-morpholinothieno[3,2-d]pyrimidine-6-yl)Methyl)(methyl)amino)pyrimidine-5-carboxylate

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Technology Process of ethyl 2-(((2-(4-(acetamidomethyl)phenyl)-4-morpholinothieno[3,2-d]pyrimidine-6-yl)Methyl)(methyl)amino)pyrimidine-5-carboxylate

There total 17 articles about ethyl 2-(((2-(4-(acetamidomethyl)phenyl)-4-morpholinothieno[3,2-d]pyrimidine-6-yl)Methyl)(methyl)amino)pyrimidine-5-carboxylate 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: 92.0%

: 1235450-93-7
N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)acetamide

: 1235450-25-5
2-[(2-chloro-4-morpholin-4-yl-thieno[3,2-d]pyrimidin-6-ylmethyl)-methyl-amino]-pyrimidine-5-carboxylic acid ethyl ester

: 1235450-95-9
ethyl 2-(((2-(4-(acetamidomethyl)phenyl)-4-morpholinothieno[3,2-d]pyrimidine-6-yl)Methyl)(methyl)amino)pyrimidine-5-carboxylate

Guidance literature:: With sodium hydrogencarbonate; bis-triphenylphosphine-palladium(II) chloride; In ethanol; water; toluene; at 130 ℃; for 2h; Inert atmosphere; Microwave irradiation;

Reference yield:

: 89793-12-4
ethyl 2-chloropyrimidine-5-carboxylate

: 1235450-95-9
ethyl 2-(((2-(4-(acetamidomethyl)phenyl)-4-morpholinothieno[3,2-d]pyrimidine-6-yl)Methyl)(methyl)amino)pyrimidine-5-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: N-ethyl-N,N-diisopropylamine / acetonitrile / 20 °C

2: sodium hydrogencarbonate / bis-triphenylphosphine-palladium(II) chloride / toluene; ethanol; water / 2 h / 130 °C / Inert atmosphere; Microwave irradiation

With sodium hydrogencarbonate; N-ethyl-N,N-diisopropylamine; bis-triphenylphosphine-palladium(II) chloride; In ethanol; water; toluene; acetonitrile;

Reference yield:

: 16233-51-5
1H-thieno[3,2-d]pyrimidine-2,4-dione

: 1235450-95-9
ethyl 2-(((2-(4-(acetamidomethyl)phenyl)-4-morpholinothieno[3,2-d]pyrimidine-6-yl)Methyl)(methyl)amino)pyrimidine-5-carboxylate

Guidance literature:: Multi-step reaction with 8 steps

1.1: trichlorophosphate / 10 h / Reflux

2.1: methanol / 1 h / 20 °C

3.1: lithium diisopropyl amide / hexane; tetrahydrofuran / 1 h / -78 °C

3.2: 11 h / -78 - 20 °C

4.1: sodium tetrahydroborate; methanol / 1 h / 20 °C

5.1: triphenylphosphine; N-Bromosuccinimide / dichloromethane / 3 h / 25 °C

6.1: ethanol / 1 h / Reflux

7.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 20 °C

8.1: sodium hydrogencarbonate / bis-triphenylphosphine-palladium(II) chloride / toluene; ethanol; water / 2 h / 130 °C / Inert atmosphere; Microwave irradiation

With methanol; sodium tetrahydroborate; N-Bromosuccinimide; sodium hydrogencarbonate; N-ethyl-N,N-diisopropylamine; triphenylphosphine; lithium diisopropyl amide; trichlorophosphate; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; methanol; ethanol; hexane; dichloromethane; water; toluene; acetonitrile;