N-[4-chloro-2-[1-[4-chloro-3-(trifluoromethyl)phenyl]pyrazole-4-carbonyl]phenyl]-3-(morpholinomethyl)benzamide

Base Information

Chemical Name:N-[4-chloro-2-[1-[4-chloro-3-(trifluoromethyl)phenyl]pyrazole-4-carbonyl]phenyl]-3-(morpholinomethyl)benzamide
CAS No.:1443255-16-0
Molecular Formula:C₂₉H₂₃Cl₂F₃N₄O₃
Molecular Weight:603.428
Hs Code.:

Synonyms:N-[4-chloro-2-[1-[4-chloro-3-(trifluoromethyl)phenyl]pyrazole-4-carbonyl]phenyl]-3-(morpholinomethyl)benzamide

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Chemical Property of N-[4-chloro-2-[1-[4-chloro-3-(trifluoromethyl)phenyl]pyrazole-4-carbonyl]phenyl]-3-(morpholinomethyl)benzamide

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Technology Process of N-[4-chloro-2-[1-[4-chloro-3-(trifluoromethyl)phenyl]pyrazole-4-carbonyl]phenyl]-3-(morpholinomethyl)benzamide

There total 7 articles about N-[4-chloro-2-[1-[4-chloro-3-(trifluoromethyl)phenyl]pyrazole-4-carbonyl]phenyl]-3-(morpholinomethyl)benzamide 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:

: 110-91-8,99108-56-2
morpholine

: 1443255-04-6
N-[4-chloro-2-[1-[4-chloro-3-(trifluoromethyl)phenyl]pyrazole-4-carbonyl]phenyl]-3-(chloromethyl)benzamide

: 1443255-16-0
N-[4-chloro-2-[1-[4-chloro-3-(trifluoromethyl)phenyl]pyrazole-4-carbonyl]phenyl]-3-(morpholinomethyl)benzamide

Guidance literature:: With potassium carbonate; In acetonitrile; at 60 ℃;

Reference yield:

: 1441141-76-9
1-[4-chloro-3-(trifluoromethyl)phenyl]pyrazole

: 1443255-16-0
N-[4-chloro-2-[1-[4-chloro-3-(trifluoromethyl)phenyl]pyrazole-4-carbonyl]phenyl]-3-(morpholinomethyl)benzamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: N-iodo-succinimide; acetic acid / 0.25 h / 150 °C / Microwave irradiation

2.1: isopropylmagnesium chloride / tetrahydrofuran / 1 h / -20 - 0 °C

2.2: 2 h / 20 °C

3.1: Dess-Martin periodane / dichloromethane / 1 h / 20 °C

4.1: iron; acetic acid / water / 2 h / 50 °C

5.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 0.25 h / 0 °C

6.1: potassium carbonate / acetonitrile / 60 °C

With N-iodo-succinimide; isopropylmagnesium chloride; iron; potassium carbonate; Dess-Martin periodane; acetic acid; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; water; acetonitrile;

Reference yield:

: 1441141-81-6
(5-chloro-2-nitro-phenyl)-[1-[4-chloro-3-(trifluoromethyl)phenyl]pyrazol-4-yl]methanol

: 1443255-16-0
N-[4-chloro-2-[1-[4-chloro-3-(trifluoromethyl)phenyl]pyrazole-4-carbonyl]phenyl]-3-(morpholinomethyl)benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: Dess-Martin periodane / dichloromethane / 1 h / 20 °C

2: iron; acetic acid / water / 2 h / 50 °C

3: N-ethyl-N,N-diisopropylamine / dichloromethane / 0.25 h / 0 °C

4: potassium carbonate / acetonitrile / 60 °C

With iron; potassium carbonate; Dess-Martin periodane; acetic acid; N-ethyl-N,N-diisopropylamine; In dichloromethane; water; acetonitrile;