2-chloro-4-[(4-fluorophenyl)sulfonylmethyl]-6-[(3S)-3-methylmorpholin-4-yl]pyrimidine

Base Information

Chemical Name:2-chloro-4-[(4-fluorophenyl)sulfonylmethyl]-6-[(3S)-3-methylmorpholin-4-yl]pyrimidine
CAS No.:1009628-46-9
Molecular Formula:C₁₆H₁₇ClFN₃O₃S
Molecular Weight:385.847
Hs Code.:

Synonyms:2-chloro-4-[(4-fluorophenyl)sulfonylmethyl]-6-[(3S)-3-methylmorpholin-4-yl]pyrimidine

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Chemical Property of 2-chloro-4-[(4-fluorophenyl)sulfonylmethyl]-6-[(3S)-3-methylmorpholin-4-yl]pyrimidine

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Technology Process of 2-chloro-4-[(4-fluorophenyl)sulfonylmethyl]-6-[(3S)-3-methylmorpholin-4-yl]pyrimidine

There total 7 articles about 2-chloro-4-[(4-fluorophenyl)sulfonylmethyl]-6-[(3S)-3-methylmorpholin-4-yl]pyrimidine 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: 76.0%

: 1009628-22-1
2-chloro-4-(iodomethyl)-6-[(3S)-3-methylmorpholin-4-yl]pyrimidine

: 824-80-6
sodium 4-fluorobenzenesulfinate

: 1009628-46-9
2-chloro-4-[(4-fluorophenyl)sulfonylmethyl]-6-[(3S)-3-methylmorpholin-4-yl]pyrimidine

Guidance literature:: In acetonitrile; at 80 ℃; for 20h; Inert atmosphere;
DOI:10.1021/jm501778s

Reference yield:

: 350595-57-2
(S)-3-methylmorpholine

: 1009628-47-0
2,4-dichloro-6-[(4-fluorophenyl)sulfonylmethyl]pyrimidine

: 1009628-46-9
2-chloro-4-[(4-fluorophenyl)sulfonylmethyl]-6-[(3S)-3-methylmorpholin-4-yl]pyrimidine

Guidance literature:: With triethylamine; In DCM; at 0 - 20 ℃; for 16.25h;

Reference yield:

: 350595-57-2
(S)-3-methylmorpholine

: 1009628-46-9
2-chloro-4-[(4-fluorophenyl)sulfonylmethyl]-6-[(3S)-3-methylmorpholin-4-yl]pyrimidine

Guidance literature:: Multi-step reaction with 5 steps

1: triethylamine / dichloromethane / 1 h / 20 °C

2: lithium borohydride / tetrahydrofuran / 1 h / 0 - 20 °C / Inert atmosphere

3: triethylamine / dichloromethane / 0.75 h / 0 - 20 °C / Inert atmosphere

4: sodium iodide / 20 h / 50 °C

5: acetonitrile / 20 h / 80 °C / Inert atmosphere

With lithium borohydride; triethylamine; sodium iodide; In tetrahydrofuran; dichloromethane; acetonitrile;
DOI:10.1021/jm501778s