2,6-difluoro-N-{3-[2-(1-methylethyl)-5-(2-{[6-(4-morpholinyl)-3-pyridinyl]amino}-4-pyrimidinyl)-1,3-thiazol-4-yl]phenyl}benzenesulfonamide

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Chemical Name:2,6-difluoro-N-{3-[2-(1-methylethyl)-5-(2-{[6-(4-morpholinyl)-3-pyridinyl]amino}-4-pyrimidinyl)-1,3-thiazol-4-yl]phenyl}benzenesulfonamide
CAS No.:1244641-64-2
Molecular Formula:C₃₁H₂₉F₂N₇O₃S₂
Molecular Weight:649.745
Hs Code.:

Synonyms:2,6-difluoro-N-{3-[2-(1-methylethyl)-5-(2-{[6-(4-morpholinyl)-3-pyridinyl]amino}-4-pyrimidinyl)-1,3-thiazol-4-yl]phenyl}benzenesulfonamide

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Chemical Property of 2,6-difluoro-N-{3-[2-(1-methylethyl)-5-(2-{[6-(4-morpholinyl)-3-pyridinyl]amino}-4-pyrimidinyl)-1,3-thiazol-4-yl]phenyl}benzenesulfonamide

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Technology Process of 2,6-difluoro-N-{3-[2-(1-methylethyl)-5-(2-{[6-(4-morpholinyl)-3-pyridinyl]amino}-4-pyrimidinyl)-1,3-thiazol-4-yl]phenyl}benzenesulfonamide

There total 6 articles about 2,6-difluoro-N-{3-[2-(1-methylethyl)-5-(2-{[6-(4-morpholinyl)-3-pyridinyl]amino}-4-pyrimidinyl)-1,3-thiazol-4-yl]phenyl}benzenesulfonamide 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: 72.0%

: 52023-68-4
6-(morpholin-4-yl)pyridin-3-amine

: 1195768-17-2
N-{3-[5-(2-chloro-4-pyrimidinyl)-2-(1-methylethyl)-1,3-thiazol-4-yl]phenyl}-2,6-difluorobenzenesulfonamide

: 1244641-64-2
2,6-difluoro-N-{3-[2-(1-methylethyl)-5-(2-{[6-(4-morpholinyl)-3-pyridinyl]amino}-4-pyrimidinyl)-1,3-thiazol-4-yl]phenyl}benzenesulfonamide

Guidance literature:: 6-(morpholin-4-yl)pyridin-3-amine; N-{3-[5-(2-chloro-4-pyrimidinyl)-2-(1-methylethyl)-1,3-thiazol-4-yl]phenyl}-2,6-difluorobenzenesulfonamide; In methanol; butan-1-ol; at 170 ℃; for 1.33333h; Inert atmosphere; microwave irradiation;

With sodium hydrogencarbonate; In water;

Reference yield:

: 4518-10-9
Methyl 3-aminobenzoate

: 1244641-64-2
2,6-difluoro-N-{3-[2-(1-methylethyl)-5-(2-{[6-(4-morpholinyl)-3-pyridinyl]amino}-4-pyrimidinyl)-1,3-thiazol-4-yl]phenyl}benzenesulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1: pyridine / dichloromethane

2: lithium hexamethyldisilazane

3: N-Bromosuccinimide / N,N-dimethyl-formamide

5: hydrogenchloride; 2,2,2-trifluoroethanol / water / 180 °C / Microwave irradiation

With pyridine; hydrogenchloride; N-Bromosuccinimide; 2,2,2-trifluoroethanol; lithium hexamethyldisilazane; In dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2011.06.021

Reference yield:

: 923880-43-7
C₁₄H₁₁F₂NO₄S

: 1244641-64-2
2,6-difluoro-N-{3-[2-(1-methylethyl)-5-(2-{[6-(4-morpholinyl)-3-pyridinyl]amino}-4-pyrimidinyl)-1,3-thiazol-4-yl]phenyl}benzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: lithium hexamethyldisilazane

2: N-Bromosuccinimide / N,N-dimethyl-formamide

4: hydrogenchloride; 2,2,2-trifluoroethanol / water / 180 °C / Microwave irradiation

With hydrogenchloride; N-Bromosuccinimide; 2,2,2-trifluoroethanol; lithium hexamethyldisilazane; In water; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2011.06.021