(R)-2-(2-{2-chloro-4-[3-(5-cyano-pyrazin-2-yl)-ureido]-5-methoxy-phenyl}-ethylcarbamoyl)-morpholine-4-carboxylic acid tert-butyl ester

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Chemical Name:(R)-2-(2-{2-chloro-4-[3-(5-cyano-pyrazin-2-yl)-ureido]-5-methoxy-phenyl}-ethylcarbamoyl)-morpholine-4-carboxylic acid tert-butyl ester
CAS No.:1437717-77-5
Molecular Formula:C₂₅H₃₀ClN₇O₆
Molecular Weight:560.009
Hs Code.:

Synonyms:(R)-2-(2-{2-chloro-4-[3-(5-cyano-pyrazin-2-yl)-ureido]-5-methoxy-phenyl}-ethylcarbamoyl)-morpholine-4-carboxylic acid tert-butyl ester

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Chemical Property of (R)-2-(2-{2-chloro-4-[3-(5-cyano-pyrazin-2-yl)-ureido]-5-methoxy-phenyl}-ethylcarbamoyl)-morpholine-4-carboxylic acid tert-butyl ester

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Technology Process of (R)-2-(2-{2-chloro-4-[3-(5-cyano-pyrazin-2-yl)-ureido]-5-methoxy-phenyl}-ethylcarbamoyl)-morpholine-4-carboxylic acid tert-butyl ester

There total 9 articles about (R)-2-(2-{2-chloro-4-[3-(5-cyano-pyrazin-2-yl)-ureido]-5-methoxy-phenyl}-ethylcarbamoyl)-morpholine-4-carboxylic acid tert-butyl 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: 54.0%

: 660851-49-0
(5-cyano-pyrazin-2-yl)-carbamic acid phenyl ester

: 1437717-69-5
(R)-2-[2-(4-amino-2-chloro-5-methoxy-phenyl)-ethylcarbamoyl]-morpholine-4-carboxylic acid tert-butyl ester

: 1437717-77-5
(R)-2-(2-{2-chloro-4-[3-(5-cyano-pyrazin-2-yl)-ureido]-5-methoxy-phenyl}-ethylcarbamoyl)-morpholine-4-carboxylic acid tert-butyl ester

Guidance literature:: In N,N-dimethyl-formamide; at 90 ℃; for 2h;

Reference yield:

: 1027833-17-5
1-bromo-2-chloro-5-fluoro-4-nitrobenzene

: 1437717-77-5
(R)-2-(2-{2-chloro-4-[3-(5-cyano-pyrazin-2-yl)-ureido]-5-methoxy-phenyl}-ethylcarbamoyl)-morpholine-4-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 7 steps

1.1: 0 °C

2.1: dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; triethylamine / propan-1-ol / 4 h / Reflux

3.1: quinoline / isopropyl alcohol / 20 h / 70 °C

4.1: water; ammonium cerium (IV) nitrate / acetonitrile / 2.5 h / 0 - 20 °C

5.1: HATU / N,N-dimethyl-formamide / 0.5 h / 0 °C

5.2: 2 h / 0 °C

6.1: zinc; ammonium chloride / methanol / 4 h / 50 °C

7.1: N,N-dimethyl-formamide / 2 h / 90 °C

With quinoline; ammonium cerium (IV) nitrate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; water; ammonium chloride; triethylamine; HATU; zinc; In methanol; propan-1-ol; N,N-dimethyl-formamide; isopropyl alcohol; acetonitrile;

Reference yield:

: 1437717-45-7
[2-(2-chloro-5-methoxy-4-nitro-phenyl)-ethyl]-(2,4-dimethoxy-benzyl)-amine

: 1437717-77-5
(R)-2-(2-{2-chloro-4-[3-(5-cyano-pyrazin-2-yl)-ureido]-5-methoxy-phenyl}-ethylcarbamoyl)-morpholine-4-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: water; ammonium cerium (IV) nitrate / acetonitrile / 2.5 h / 0 - 20 °C

2.1: HATU / N,N-dimethyl-formamide / 0.5 h / 0 °C

2.2: 2 h / 0 °C

3.1: zinc; ammonium chloride / methanol / 4 h / 50 °C

4.1: N,N-dimethyl-formamide / 2 h / 90 °C

With ammonium cerium (IV) nitrate; water; ammonium chloride; HATU; zinc; In methanol; N,N-dimethyl-formamide; acetonitrile;