2-propen-1-yl [3-[5-(2-chloro-4-pyrimidinyl)-2-(1-methylethyl)-1,3-thiazol-4-yl]-2-(methyloxy)phenyl]carbamate

Base Information

Chemical Name:2-propen-1-yl [3-[5-(2-chloro-4-pyrimidinyl)-2-(1-methylethyl)-1,3-thiazol-4-yl]-2-(methyloxy)phenyl]carbamate
CAS No.:1195768-89-8
Molecular Formula:C₂₁H₂₁ClN₄O₃S
Molecular Weight:444.942
Hs Code.:

Synonyms:2-propen-1-yl [3-[5-(2-chloro-4-pyrimidinyl)-2-(1-methylethyl)-1,3-thiazol-4-yl]-2-(methyloxy)phenyl]carbamate

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Chemical Property of 2-propen-1-yl [3-[5-(2-chloro-4-pyrimidinyl)-2-(1-methylethyl)-1,3-thiazol-4-yl]-2-(methyloxy)phenyl]carbamate

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Technology Process of 2-propen-1-yl [3-[5-(2-chloro-4-pyrimidinyl)-2-(1-methylethyl)-1,3-thiazol-4-yl]-2-(methyloxy)phenyl]carbamate

There total 6 articles about 2-propen-1-yl [3-[5-(2-chloro-4-pyrimidinyl)-2-(1-methylethyl)-1,3-thiazol-4-yl]-2-(methyloxy)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: 63.8%

: 13515-65-6
thioisobutyramide

: 1195768-88-7
2-propen-1-yl [3-[(2-chloro-4-pyrimidinyl)acetyl]-2-(methyloxy)phenyl]carbamate

: 1195768-89-8
2-propen-1-yl [3-[5-(2-chloro-4-pyrimidinyl)-2-(1-methylethyl)-1,3-thiazol-4-yl]-2-(methyloxy)phenyl]carbamate

Guidance literature:: 2-propen-1-yl [3-[(2-chloro-4-pyrimidinyl)acetyl]-2-(methyloxy)phenyl]carbamate; With N-Bromosuccinimide; In dichloromethane; at 20 ℃; for 0.5h;

thioisobutyramide; In dimethyl sulfoxide; at 20 ℃; for 1h;

Reference yield:

: 22621-41-6
2-hydroxy-3-nitro-benzoic acid methyl ester

: 1195768-89-8
2-propen-1-yl [3-[5-(2-chloro-4-pyrimidinyl)-2-(1-methylethyl)-1,3-thiazol-4-yl]-2-(methyloxy)phenyl]carbamate

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 20 - 45 °C

2.1: hydrogen / nickel / methanol / 3.5 h / 25 °C / 2585.81 Torr

3.1: sodium hydrogencarbonate / tetrahydrofuran; water / 0 - 20 °C

4.1: lithium hexamethyldisilazane / tetrahydrofuran / -10 - 0 °C

4.2: 1.33 h / 0 - 20 °C

5.1: N-Bromosuccinimide / dichloromethane / 0.5 h / 20 °C

5.2: 1 h / 20 °C

With N-Bromosuccinimide; hydrogen; sodium hydrogencarbonate; potassium carbonate; lithium hexamethyldisilazane; nickel; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 85-38-1
3-nitrosalicylic acid

: 1195768-89-8
2-propen-1-yl [3-[5-(2-chloro-4-pyrimidinyl)-2-(1-methylethyl)-1,3-thiazol-4-yl]-2-(methyloxy)phenyl]carbamate

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 20 °C

2.1: potassium carbonate / N,N-dimethyl-formamide / 20 - 45 °C

3.1: hydrogen / nickel / methanol / 3.5 h / 25 °C / 2585.81 Torr

4.1: sodium hydrogencarbonate / tetrahydrofuran; water / 0 - 20 °C

5.1: lithium hexamethyldisilazane / tetrahydrofuran / -10 - 0 °C

5.2: 1.33 h / 0 - 20 °C

6.1: N-Bromosuccinimide / dichloromethane / 0.5 h / 20 °C

6.2: 1 h / 20 °C

With N-Bromosuccinimide; hydrogen; sodium hydrogencarbonate; potassium carbonate; lithium hexamethyldisilazane; nickel; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;