methyl-5-[2-bromo-4-(1-{2-[4-(N-hydroxycarbamimidoyl)-phenylcarbamoyl]-acetylamino}-ethyl)-phenoxy]-nicotinate

Base Information

Chemical Name:methyl-5-[2-bromo-4-(1-{2-[4-(N-hydroxycarbamimidoyl)-phenylcarbamoyl]-acetylamino}-ethyl)-phenoxy]-nicotinate
CAS No.:1100767-38-1
Molecular Formula:C₂₅H₂₄BrN₅O₆
Molecular Weight:570.399
Hs Code.:

Synonyms:methyl-5-[2-bromo-4-(1-{2-[4-(N-hydroxycarbamimidoyl)-phenylcarbamoyl]-acetylamino}-ethyl)-phenoxy]-nicotinate

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Chemical Property of methyl-5-[2-bromo-4-(1-{2-[4-(N-hydroxycarbamimidoyl)-phenylcarbamoyl]-acetylamino}-ethyl)-phenoxy]-nicotinate

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Technology Process of methyl-5-[2-bromo-4-(1-{2-[4-(N-hydroxycarbamimidoyl)-phenylcarbamoyl]-acetylamino}-ethyl)-phenoxy]-nicotinate

There total 8 articles about methyl-5-[2-bromo-4-(1-{2-[4-(N-hydroxycarbamimidoyl)-phenylcarbamoyl]-acetylamino}-ethyl)-phenoxy]-nicotinate 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: 81.0%

: 1100767-36-9
methyl-5-(2-bromo-4-{1-[2-(4-cyano-phenylcarbamoyl)-acetylamino]-ethyl}-phenoxy)-nicotinate

: 1100767-38-1
methyl-5-[2-bromo-4-(1-{2-[4-(N-hydroxycarbamimidoyl)-phenylcarbamoyl]-acetylamino}-ethyl)-phenoxy]-nicotinate

Guidance literature:: With hydroxylamine hydrochloride; triethylamine; In isopropyl alcohol; at 70 ℃; for 4h;

Reference yield:

: 1007-15-4
4-fluoro-3-bromoacetophenone

: 1100767-38-1
methyl-5-[2-bromo-4-(1-{2-[4-(N-hydroxycarbamimidoyl)-phenylcarbamoyl]-acetylamino}-ethyl)-phenoxy]-nicotinate

Guidance literature:: Multi-step reaction with 4 steps

1.1: 40% potassium fluoride/alumina; 18-crown-6 ether / acetonitrile / 72 h / Heating / reflux

2.1: ammonium acetate / methanol / 20 °C

2.2: 6 h / Heating / reflux

3.1: 1-hydroxy-7-aza-benzotriazole; N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 48 h / 20 °C

4.1: hydroxylamine hydrochloride; triethylamine / isopropyl alcohol / 4 h / 70 °C

With 1-hydroxy-7-aza-benzotriazole; 18-crown-6 ether; 40% potassium fluoride/alumina; hydroxylamine hydrochloride; ammonium acetate; triethylamine; N-ethyl-N,N-diisopropylamine; HATU; In methanol; N,N-dimethyl-formamide; isopropyl alcohol; acetonitrile;

Reference yield:

: 1100767-21-2
2-[4-cyano-phenylcarbamoyl]-acetic acid

: 1100767-38-1
methyl-5-[2-bromo-4-(1-{2-[4-(N-hydroxycarbamimidoyl)-phenylcarbamoyl]-acetylamino}-ethyl)-phenoxy]-nicotinate

Guidance literature:: Multi-step reaction with 2 steps

1: 1-hydroxy-7-aza-benzotriazole; N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 48 h / 20 °C

2: hydroxylamine hydrochloride; triethylamine / isopropyl alcohol / 4 h / 70 °C

With 1-hydroxy-7-aza-benzotriazole; hydroxylamine hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; isopropyl alcohol;