N-{2-chloro-3-[5-(2-chloro-4-pyrimidinyl)-2-(1-methyl-4-piperidinyl)-1,3-thiazol-4-yl]phenyl}-1-propanesulfonamide

Base Information

Chemical Name:N-{2-chloro-3-[5-(2-chloro-4-pyrimidinyl)-2-(1-methyl-4-piperidinyl)-1,3-thiazol-4-yl]phenyl}-1-propanesulfonamide
CAS No.:1307272-77-0
Molecular Formula:C₂₂H₂₅Cl₂N₅O₂S₂
Molecular Weight:526.511
Hs Code.:

Synonyms:N-{2-chloro-3-[5-(2-chloro-4-pyrimidinyl)-2-(1-methyl-4-piperidinyl)-1,3-thiazol-4-yl]phenyl}-1-propanesulfonamide

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Chemical Property of N-{2-chloro-3-[5-(2-chloro-4-pyrimidinyl)-2-(1-methyl-4-piperidinyl)-1,3-thiazol-4-yl]phenyl}-1-propanesulfonamide

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Technology Process of N-{2-chloro-3-[5-(2-chloro-4-pyrimidinyl)-2-(1-methyl-4-piperidinyl)-1,3-thiazol-4-yl]phenyl}-1-propanesulfonamide

There total 8 articles about N-{2-chloro-3-[5-(2-chloro-4-pyrimidinyl)-2-(1-methyl-4-piperidinyl)-1,3-thiazol-4-yl]phenyl}-1-propanesulfonamide 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: 36.0%

: 50-00-0,30525-89-4,61233-19-0
formaldehyd

: 1307272-76-9
N-{2-chloro-3-[5-(2-chloro-4-pyrimidinyl)-2-(4-piperidinyl)-1,3-thiazol-4-yl]phenyl}-1-propanesulfonamide

: 1307272-77-0
N-{2-chloro-3-[5-(2-chloro-4-pyrimidinyl)-2-(1-methyl-4-piperidinyl)-1,3-thiazol-4-yl]phenyl}-1-propanesulfonamide

Guidance literature:: With sodium tris(acetoxy)borohydride; In 1,2-dichloro-ethane; at 20 ℃; Inert atmosphere;

Reference yield:

: 120100-15-4
methyl 3-amino-2-chlorobenzoate

: 1307272-77-0
N-{2-chloro-3-[5-(2-chloro-4-pyrimidinyl)-2-(1-methyl-4-piperidinyl)-1,3-thiazol-4-yl]phenyl}-1-propanesulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: pyridine / 6.5 h / 0 - 30 °C / Inert atmosphere

2.1: lithium hexamethyldisilazane / tetrahydrofuran / 3 h / -30 - -10 °C / Inert atmosphere

2.2: -10 - 20 °C / Inert atmosphere

3.1: N-Bromosuccinimide / ISOPROPYLAMIDE / 1.33 h / 20 °C / Inert atmosphere

3.2: 72 h / 20 °C / Inert atmosphere

4.1: trifluoroacetic acid / dichloromethane / 1 h / 20 °C / Inert atmosphere

5.1: sodium tris(acetoxy)borohydride / 1,2-dichloro-ethane / 20 °C / Inert atmosphere

With pyridine; N-Bromosuccinimide; sodium tris(acetoxy)borohydride; trifluoroacetic acid; lithium hexamethyldisilazane; In tetrahydrofuran; dichloromethane; ISOPROPYLAMIDE; 1,2-dichloro-ethane;

Reference yield:

: 214834-18-1
tert-butyl 4-carbamothioylpiperidine-1-carboxylate

: 1307272-77-0
N-{2-chloro-3-[5-(2-chloro-4-pyrimidinyl)-2-(1-methyl-4-piperidinyl)-1,3-thiazol-4-yl]phenyl}-1-propanesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: N-Bromosuccinimide / ISOPROPYLAMIDE / 1.33 h / 20 °C / Inert atmosphere

1.2: 72 h / 20 °C / Inert atmosphere

2.1: trifluoroacetic acid / dichloromethane / 1 h / 20 °C / Inert atmosphere

3.1: sodium tris(acetoxy)borohydride / 1,2-dichloro-ethane / 20 °C / Inert atmosphere

With N-Bromosuccinimide; sodium tris(acetoxy)borohydride; trifluoroacetic acid; In dichloromethane; ISOPROPYLAMIDE; 1,2-dichloro-ethane;