N-{4-[3-(4,5-bis-hydroxymethyl-imidazol-1-yl)-propyl]-phenyl}-4-(quinolin-4-ylamino)-benzamide

Base Information

Chemical Name:N-{4-[3-(4,5-bis-hydroxymethyl-imidazol-1-yl)-propyl]-phenyl}-4-(quinolin-4-ylamino)-benzamide
CAS No.:218629-11-9
Molecular Formula:C₃₀H₂₉N₅O₃
Molecular Weight:507.592
Hs Code.:

<i>N</i>-{4-[3-(4,5-bis-hydroxymethyl-imidazol-1-yl)-propyl]-phenyl}-4-(quinolin-4-ylamino)-benzamide

Synonyms:N-{4-[3-(4,5-bis-hydroxymethyl-imidazol-1-yl)-propyl]-phenyl}-4-(quinolin-4-ylamino)-benzamide

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Chemical Property of N-{4-[3-(4,5-bis-hydroxymethyl-imidazol-1-yl)-propyl]-phenyl}-4-(quinolin-4-ylamino)-benzamide

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Technology Process of N-{4-[3-(4,5-bis-hydroxymethyl-imidazol-1-yl)-propyl]-phenyl}-4-(quinolin-4-ylamino)-benzamide

There total 7 articles about N-{4-[3-(4,5-bis-hydroxymethyl-imidazol-1-yl)-propyl]-phenyl}-4-(quinolin-4-ylamino)-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: 63.0%

: 218629-09-5
dimethyl 1-<3-<4-<4-(4-quinolinylamino)benzamido>phenyl>propyl>imidazole-4,5-dicarboxylate

: 218629-11-9
N-{4-[3-(4,5-bis-hydroxymethyl-imidazol-1-yl)-propyl]-phenyl}-4-(quinolin-4-ylamino)-benzamide

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; at 20 ℃; for 2h;
DOI:10.1021/jm9803119

Reference yield:

: 3304-70-9
dimethyl imidazole-4,5-dicarboxylate

: 218629-11-9
N-{4-[3-(4,5-bis-hydroxymethyl-imidazol-1-yl)-propyl]-phenyl}-4-(quinolin-4-ylamino)-benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: 88 percent / K₂CO₃ / dimethylformamide / 2.5 h / 70 °C

2: 95 percent / H₂ / Pt/C / methanol / 2 h / 2585.74 Torr

3: diisopropylethylamine / dimethylformamide / 6 h / 20 °C

4: 63 percent / LiAlH₄ / tetrahydrofuran / 2 h / 20 °C

With lithium aluminium tetrahydride; hydrogen; potassium carbonate; N-ethyl-N,N-diisopropylamine; platinum on activated charcoal; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1021/jm9803119

Reference yield:

: 53712-77-9
1-bromo-3-(4-nitrophenyl)propane

: 218629-11-9
N-{4-[3-(4,5-bis-hydroxymethyl-imidazol-1-yl)-propyl]-phenyl}-4-(quinolin-4-ylamino)-benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: 88 percent / K₂CO₃ / dimethylformamide / 2.5 h / 70 °C

2: 95 percent / H₂ / Pt/C / methanol / 2 h / 2585.74 Torr

3: diisopropylethylamine / dimethylformamide / 6 h / 20 °C

4: 63 percent / LiAlH₄ / tetrahydrofuran / 2 h / 20 °C

With lithium aluminium tetrahydride; hydrogen; potassium carbonate; N-ethyl-N,N-diisopropylamine; platinum on activated charcoal; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1021/jm9803119