(R)-tert-butyl 3-((R)-(4-chloro-3-fluorophenyl)(4-(2-(methylthio)pyrimidin-4-yl)-2-oxopyridin-1(2H)-yl)methyl)pyrrolidine-1-carboxylate

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Chemical Name:(R)-tert-butyl 3-((R)-(4-chloro-3-fluorophenyl)(4-(2-(methylthio)pyrimidin-4-yl)-2-oxopyridin-1(2H)-yl)methyl)pyrrolidine-1-carboxylate
CAS No.:1453854-02-8
Molecular Formula:C₂₆H₂₈ClFN₄O₃S
Molecular Weight:531.051
Hs Code.:

Synonyms:(R)-tert-butyl 3-((R)-(4-chloro-3-fluorophenyl)(4-(2-(methylthio)pyrimidin-4-yl)-2-oxopyridin-1(2H)-yl)methyl)pyrrolidine-1-carboxylate

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Chemical Property of (R)-tert-butyl 3-((R)-(4-chloro-3-fluorophenyl)(4-(2-(methylthio)pyrimidin-4-yl)-2-oxopyridin-1(2H)-yl)methyl)pyrrolidine-1-carboxylate

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Technology Process of (R)-tert-butyl 3-((R)-(4-chloro-3-fluorophenyl)(4-(2-(methylthio)pyrimidin-4-yl)-2-oxopyridin-1(2H)-yl)methyl)pyrrolidine-1-carboxylate

There total 7 articles about (R)-tert-butyl 3-((R)-(4-chloro-3-fluorophenyl)(4-(2-(methylthio)pyrimidin-4-yl)-2-oxopyridin-1(2H)-yl)methyl)pyrrolidine-1-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: 9.0%

: 1453854-00-6
(3R)-tert-butyl-3-((4-chloro-3-fluorophenyl)(hydroxy)methyl)pyrrolidine-1-carboxylate

: 1453851-57-4
4-(2-(methylthio)pyrimidin-4-yl)pyridin-2(1H)-one

: 1453854-04-0
(R)-tert-butyl-3-((S)-(4-chloro-3-fluorophenyl)(4-(2-(methylthio)pyrimidin-4-yl)-2-oxopyridin-1(2H)-yl)methyl)pyrrolidine-1-carboxylate

: 1453854-02-8
(R)-tert-butyl 3-((R)-(4-chloro-3-fluorophenyl)(4-(2-(methylthio)pyrimidin-4-yl)-2-oxopyridin-1(2H)-yl)methyl)pyrrolidine-1-carboxylate

Guidance literature:: (3R)-tert-butyl-3-((4-chloro-3-fluorophenyl)(hydroxy)methyl)pyrrolidine-1-carboxylate; With di-isopropyl azodicarboxylate; triphenylphosphine; In dichloromethane; at 0 - 20 ℃; for 0.25h; Inert atmosphere;

4-(2-(methylthio)pyrimidin-4-yl)pyridin-2(1H)-one; at 20 ℃; for 16h;

Reference yield:

: 1453853-98-9
(R)-tert-butyl 3-(4-chloro-3-fluorobenzoyl)pyrrolidine-1-carboxylate

: 1453854-02-8
(R)-tert-butyl 3-((R)-(4-chloro-3-fluorophenyl)(4-(2-(methylthio)pyrimidin-4-yl)-2-oxopyridin-1(2H)-yl)methyl)pyrrolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: L-Selectride / tetrahydrofuran / 0.5 h / -78 °C / Inert atmosphere

2.1: triphenylphosphine; di-isopropyl azodicarboxylate / dichloromethane / 0.25 h / 0 - 20 °C / Inert atmosphere

2.2: 16 h / 20 °C

With di-isopropyl azodicarboxylate; L-Selectride; triphenylphosphine; In tetrahydrofuran; dichloromethane; 2.1: |Mitsunobu Displacement;

Reference yield:

: 1204677-54-2
(R)-tert-butyl-3-(methoxy(methyl)carbamoyl)pyrrolidine-1-carboxylate

: 1453854-02-8
(R)-tert-butyl 3-((R)-(4-chloro-3-fluorophenyl)(4-(2-(methylthio)pyrimidin-4-yl)-2-oxopyridin-1(2H)-yl)methyl)pyrrolidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: tetrahydrofuran / 1.5 h / 0 °C / Inert atmosphere

2.1: L-Selectride / tetrahydrofuran / 0.5 h / -78 °C / Inert atmosphere

3.1: triphenylphosphine; di-isopropyl azodicarboxylate / dichloromethane / 0.25 h / 0 - 20 °C / Inert atmosphere

3.2: 16 h / 20 °C

With di-isopropyl azodicarboxylate; L-Selectride; triphenylphosphine; In tetrahydrofuran; dichloromethane; 3.1: |Mitsunobu Displacement;