5-bromo-2-{[(4-fluorophenyl)methyl]oxy}-N-(3-methyl-4-isoxazolyl)-4-(4-morpholinylmethyl)benzamide

Base Information

Chemical Name:5-bromo-2-{[(4-fluorophenyl)methyl]oxy}-N-(3-methyl-4-isoxazolyl)-4-(4-morpholinylmethyl)benzamide
CAS No.:1362818-03-8
Molecular Formula:C₂₃H₂₃BrFN₃O₄
Molecular Weight:504.356
Hs Code.:

Synonyms:5-bromo-2-{[(4-fluorophenyl)methyl]oxy}-N-(3-methyl-4-isoxazolyl)-4-(4-morpholinylmethyl)benzamide

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Chemical Property of 5-bromo-2-{[(4-fluorophenyl)methyl]oxy}-N-(3-methyl-4-isoxazolyl)-4-(4-morpholinylmethyl)benzamide

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Technology Process of 5-bromo-2-{[(4-fluorophenyl)methyl]oxy}-N-(3-methyl-4-isoxazolyl)-4-(4-morpholinylmethyl)benzamide

There total 9 articles about 5-bromo-2-{[(4-fluorophenyl)methyl]oxy}-N-(3-methyl-4-isoxazolyl)-4-(4-morpholinylmethyl)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:

: 354795-62-3
3-methylisoxazol-4-ylamine

: 1362819-73-5
5-bromo-2-{[(4-fluorophenyl)methyl]oxy}-4-(4-morpholinylmethyl)benzoic acid

: 1362818-03-8
5-bromo-2-{[(4-fluorophenyl)methyl]oxy}-N-(3-methyl-4-isoxazolyl)-4-(4-morpholinylmethyl)benzamide

Guidance literature:: With 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; for 18h;

Reference yield:

: 50-85-1
2-hydroxy-p-toluic acid

: 1362818-03-8
5-bromo-2-{[(4-fluorophenyl)methyl]oxy}-N-(3-methyl-4-isoxazolyl)-4-(4-morpholinylmethyl)benzamide

Guidance literature:: Multi-step reaction with 9 steps

1: thionyl chloride / 24 h / 50 °C

2: bromine / chloroform / 1 h / 0 °C

3: pyridine / 4 h

4: N-Bromosuccinimide / dibenzoyl peroxide / tetrachloromethane / 18 h / Reflux

5: triethylamine / acetone / 0.5 h

6: water; lithium hydroxide / tetrahydrofuran / 1.5 h / 50 °C

7: potassium carbonate / N,N-dimethyl-formamide / 20 °C

8: water; lithium hydroxide / tetrahydrofuran / 4 h / 50 °C

9: 1-hydroxy-7-aza-benzotriazole; N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 18 h

With pyridine; N-Bromosuccinimide; thionyl chloride; 1-hydroxy-7-aza-benzotriazole; water; bromine; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; lithium hydroxide; dibenzoyl peroxide; In tetrahydrofuran; tetrachloromethane; chloroform; N,N-dimethyl-formamide; acetone;

Reference yield:

: 4670-56-8
methyl 2-hydroxy-4-methylbenzoate

: 1362818-03-8
5-bromo-2-{[(4-fluorophenyl)methyl]oxy}-N-(3-methyl-4-isoxazolyl)-4-(4-morpholinylmethyl)benzamide

Guidance literature:: Multi-step reaction with 8 steps

1: bromine / chloroform / 1 h / 0 °C

2: pyridine / 4 h

3: N-Bromosuccinimide / dibenzoyl peroxide / tetrachloromethane / 18 h / Reflux

4: triethylamine / acetone / 0.5 h

5: water; lithium hydroxide / tetrahydrofuran / 1.5 h / 50 °C

6: potassium carbonate / N,N-dimethyl-formamide / 20 °C

7: water; lithium hydroxide / tetrahydrofuran / 4 h / 50 °C

8: 1-hydroxy-7-aza-benzotriazole; N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 18 h

With pyridine; N-Bromosuccinimide; 1-hydroxy-7-aza-benzotriazole; water; bromine; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; lithium hydroxide; dibenzoyl peroxide; In tetrahydrofuran; tetrachloromethane; chloroform; N,N-dimethyl-formamide; acetone;