4-(2-chlorophenyl)-1-[2-(isobutyrylamino)-5-methylpyridin-4-yl]-1H-pyrrole-3-carboxamide

Base Information

Chemical Name:4-(2-chlorophenyl)-1-[2-(isobutyrylamino)-5-methylpyridin-4-yl]-1H-pyrrole-3-carboxamide
CAS No.:1445888-71-0
Molecular Formula:C₂₁H₂₁ClN₄O₂
Molecular Weight:396.876
Hs Code.:

Synonyms:4-(2-chlorophenyl)-1-[2-(isobutyrylamino)-5-methylpyridin-4-yl]-1H-pyrrole-3-carboxamide

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Chemical Property of 4-(2-chlorophenyl)-1-[2-(isobutyrylamino)-5-methylpyridin-4-yl]-1H-pyrrole-3-carboxamide

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Technology Process of 4-(2-chlorophenyl)-1-[2-(isobutyrylamino)-5-methylpyridin-4-yl]-1H-pyrrole-3-carboxamide

There total 12 articles about 4-(2-chlorophenyl)-1-[2-(isobutyrylamino)-5-methylpyridin-4-yl]-1H-pyrrole-3-carboxamide 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: 76.0%

: 1445890-90-3
1-(2-amino-5-methylpyridin-4-yl)-4-(2-chlorophenyl)-1H-pyrrole-3-carboxamide

: 79-30-1
isobutyryl chloride

: 1445888-71-0
4-(2-chlorophenyl)-1-[2-(isobutyrylamino)-5-methylpyridin-4-yl]-1H-pyrrole-3-carboxamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; sodium hydroxide; In methanol; dichloromethane; at 0 ℃; for 1h;

Reference yield:

: 1188163-01-0
ethyl 4-(2-chlorophenyl)-1H-pyrrole-3-carboxylate

: 1445888-71-0
4-(2-chlorophenyl)-1-[2-(isobutyrylamino)-5-methylpyridin-4-yl]-1H-pyrrole-3-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: trans-N,N'-dimethyl-1,2-cyclohexyldiamine; copper(l) iodide; potassium carbonate / 1,4-dioxane / 48 h / 105 °C / Sealed tube

2: sodium hydroxide; water / tetrahydrofuran; methanol / 96 h / 50 °C

3: ammonia; HATU; N-ethyl-N,N-diisopropylamine / dichloromethane; 1,4-dioxane / 3 h / 20 °C

4: sodium hydroxide; N-ethyl-N,N-diisopropylamine / dichloromethane; methanol / 1 h / 0 °C

With trans-N,N'-dimethyl-1,2-cyclohexyldiamine; copper(l) iodide; ammonia; water; potassium carbonate; N-ethyl-N,N-diisopropylamine; HATU; sodium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane;

Reference yield:

: 24393-51-9
(E)-ethyl 2-chlorocinnamate

: 1445888-71-0
4-(2-chlorophenyl)-1-[2-(isobutyrylamino)-5-methylpyridin-4-yl]-1H-pyrrole-3-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1: sodium t-butanolate / tetrahydrofuran / 3.33 h / -40 - 20 °C

2: trans-N,N'-dimethyl-1,2-cyclohexyldiamine; copper(l) iodide; potassium carbonate / 1,4-dioxane / 48 h / 105 °C / Sealed tube

3: sodium hydroxide; water / tetrahydrofuran; methanol / 96 h / 50 °C

4: ammonia; HATU; N-ethyl-N,N-diisopropylamine / dichloromethane; 1,4-dioxane / 3 h / 20 °C

5: sodium hydroxide; N-ethyl-N,N-diisopropylamine / dichloromethane; methanol / 1 h / 0 °C

With trans-N,N'-dimethyl-1,2-cyclohexyldiamine; copper(l) iodide; ammonia; water; potassium carbonate; N-ethyl-N,N-diisopropylamine; HATU; sodium hydroxide; sodium t-butanolate; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane;