1-(2-bromo-4-isopropyl-phenyl)-6-methyl-4-morpholin-4-yl-1H-pyrrolo[2,3-b]pyridine-3-carbonitrile

Base Information

Chemical Name:1-(2-bromo-4-isopropyl-phenyl)-6-methyl-4-morpholin-4-yl-1H-pyrrolo[2,3-b]pyridine-3-carbonitrile
CAS No.:223719-77-5
Molecular Formula:C₂₂H₂₃BrN₄O
Molecular Weight:439.355
Hs Code.:

1-(2-bromo-4-isopropyl-phenyl)-6-methyl-4-morpholin-4-yl-1<i>H</i>-pyrrolo[2,3-<i>b</i>]pyridine-3-carbonitrile

Synonyms:1-(2-bromo-4-isopropyl-phenyl)-6-methyl-4-morpholin-4-yl-1H-pyrrolo[2,3-b]pyridine-3-carbonitrile

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Chemical Property of 1-(2-bromo-4-isopropyl-phenyl)-6-methyl-4-morpholin-4-yl-1H-pyrrolo[2,3-b]pyridine-3-carbonitrile

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Technology Process of 1-(2-bromo-4-isopropyl-phenyl)-6-methyl-4-morpholin-4-yl-1H-pyrrolo[2,3-b]pyridine-3-carbonitrile

There total 6 articles about 1-(2-bromo-4-isopropyl-phenyl)-6-methyl-4-morpholin-4-yl-1H-pyrrolo[2,3-b]pyridine-3-carbonitrile 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:

: 51605-97-1
2-bromo-4-isopropylaniline

: 223719-77-5
1-(2-bromo-4-isopropyl-phenyl)-6-methyl-4-morpholin-4-yl-1H-pyrrolo[2,3-b]pyridine-3-carbonitrile

Guidance literature:: Multi-step reaction with 5 steps

1: 40 percent / gl. AcOH / ethanol / 2 h / Heating

2: 59 percent / t-BuOK / ethanol; tetrahydrofuran / 16 h / Ambient temperature

3: 10 percent / conc. HCl / ethanol / 16 h / Heating

4: 71 percent / 3-chloroperoxybenzoic acid / CHCl₃ / 6 h / Heating

5: 1.) triflic anhydride / 1.) CHCl₃, RT, 20 min, 2.) CHCl₃, reflux, 2h

With hydrogenchloride; trifluoromethylsulfonic anhydride; potassium tert-butylate; acetic acid; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; ethanol; chloroform;
DOI:10.1021/jm980223o

Reference yield:

: potassium salt of formylsuccinonitrile

: 223719-77-5
1-(2-bromo-4-isopropyl-phenyl)-6-methyl-4-morpholin-4-yl-1H-pyrrolo[2,3-b]pyridine-3-carbonitrile

Guidance literature:: Multi-step reaction with 5 steps

1: 40 percent / gl. AcOH / ethanol / 2 h / Heating

2: 59 percent / t-BuOK / ethanol; tetrahydrofuran / 16 h / Ambient temperature

3: 10 percent / conc. HCl / ethanol / 16 h / Heating

4: 71 percent / 3-chloroperoxybenzoic acid / CHCl₃ / 6 h / Heating

5: 1.) triflic anhydride / 1.) CHCl₃, RT, 20 min, 2.) CHCl₃, reflux, 2h

With hydrogenchloride; trifluoromethylsulfonic anhydride; potassium tert-butylate; acetic acid; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; ethanol; chloroform;
DOI:10.1021/jm980223o

Reference yield:

: 169883-12-9
1-(2-bromo-4-isopropylphenyl)-2-amino-4-cyanopyrrole

: 223719-77-5
1-(2-bromo-4-isopropyl-phenyl)-6-methyl-4-morpholin-4-yl-1H-pyrrolo[2,3-b]pyridine-3-carbonitrile

Guidance literature:: Multi-step reaction with 3 steps

1: 10 percent / conc. HCl / ethanol / 16 h / Heating

2: 71 percent / 3-chloroperoxybenzoic acid / CHCl₃ / 6 h / Heating

3: 1.) triflic anhydride / 1.) CHCl₃, RT, 20 min, 2.) CHCl₃, reflux, 2h

With hydrogenchloride; trifluoromethylsulfonic anhydride; 3-chloro-benzenecarboperoxoic acid; In ethanol; chloroform;
DOI:10.1021/jm980223o