2-(4-(2-(5-cyanothiophen-2-yl)-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yloxy)phenyl)acetic acid methyl ester

Base Information

Chemical Name:2-(4-(2-(5-cyanothiophen-2-yl)-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yloxy)phenyl)acetic acid methyl ester
CAS No.:1621363-38-9
Molecular Formula:C₂₁H₁₇N₃O₃S
Molecular Weight:391.45
Hs Code.:

Synonyms:2-(4-(2-(5-cyanothiophen-2-yl)-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yloxy)phenyl)acetic acid methyl ester

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Chemical Property of 2-(4-(2-(5-cyanothiophen-2-yl)-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yloxy)phenyl)acetic acid methyl ester

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Technology Process of 2-(4-(2-(5-cyanothiophen-2-yl)-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yloxy)phenyl)acetic acid methyl ester

There total 5 articles about 2-(4-(2-(5-cyanothiophen-2-yl)-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yloxy)phenyl)acetic acid methyl ester 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: 69.0%

: 305832-67-1
5-cyanothiophen-2-ylboronic acid

: 1621363-37-8
2-(4-(2-bromo-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yloxy)phenyl)acetic acid methyl ester

: 1621363-38-9
2-(4-(2-(5-cyanothiophen-2-yl)-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yloxy)phenyl)acetic acid methyl ester

Guidance literature:: With bis-triphenylphosphine-palladium(II) chloride; potassium fluoride; In tetrahydrofuran; at 90 ℃;

Reference yield:

: 5466-43-3
2,4-dichloro-6,7-dihydro-5H-cyclopentapyrimidine

: 1621363-38-9
2-(4-(2-(5-cyanothiophen-2-yl)-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yloxy)phenyl)acetic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 1,8-diazabicyclo[5.4.0]undec-7-ene / 1,4-dioxane / 2 h / Reflux

2: hydrogen bromide; acetic acid / 4 h / 20 °C

3: potassium fluoride; bis-triphenylphosphine-palladium(II) chloride / tetrahydrofuran / 90 °C

With bis-triphenylphosphine-palladium(II) chloride; potassium fluoride; hydrogen bromide; acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; 1,4-dioxane;

Reference yield:

: 10472-24-9,265317-94-0
methyl 2-oxocyclopentane-1-carboxylate

: 1621363-38-9
2-(4-(2-(5-cyanothiophen-2-yl)-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yloxy)phenyl)acetic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: chloro-trimethyl-silane / N,N-dimethyl-formamide / 0 - 20 °C

2: trichlorophosphate; sodium hydrogencarbonate / 24 h / 85 - 100 °C / Cooling with ice

3: 1,8-diazabicyclo[5.4.0]undec-7-ene / 1,4-dioxane / 2 h / Reflux

4: hydrogen bromide; acetic acid / 4 h / 20 °C

5: potassium fluoride; bis-triphenylphosphine-palladium(II) chloride / tetrahydrofuran / 90 °C

With bis-triphenylphosphine-palladium(II) chloride; potassium fluoride; chloro-trimethyl-silane; hydrogen bromide; sodium hydrogencarbonate; acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; trichlorophosphate; In tetrahydrofuran; 1,4-dioxane; N,N-dimethyl-formamide;