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2-[(1R)-1-({[(6R)-6-(5-Chloro-2-methoxybenzyl)-3,7-dioxo-1,4-diazepan-1-yl]carbonyl}amino)propyl]-4-oxazolcarboxylic acid

Base Information
  • Chemical Name:2-[(1R)-1-({[(6R)-6-(5-Chloro-2-methoxybenzyl)-3,7-dioxo-1,4-diazepan-1-yl]carbonyl}amino)propyl]-4-oxazolcarboxylic acid
  • CAS No.:1444198-69-9
  • Molecular Formula:C21H23ClN4O7
  • Molecular Weight:478.889
  • Hs Code.:
2-[(1R)-1-({[(6R)-6-(5-Chloro-2-methoxybenzyl)-3,7-dioxo-1,4-diazepan-1-yl]carbonyl}amino)propyl]-4-oxazolcarboxylic acid

Synonyms:2-[(1R)-1-({[(6R)-6-(5-Chloro-2-methoxybenzyl)-3,7-dioxo-1,4-diazepan-1-yl]carbonyl}amino)propyl]-4-oxazolcarboxylic acid

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Chemical Property of 2-[(1R)-1-({[(6R)-6-(5-Chloro-2-methoxybenzyl)-3,7-dioxo-1,4-diazepan-1-yl]carbonyl}amino)propyl]-4-oxazolcarboxylic acid
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Technology Process of 2-[(1R)-1-({[(6R)-6-(5-Chloro-2-methoxybenzyl)-3,7-dioxo-1,4-diazepan-1-yl]carbonyl}amino)propyl]-4-oxazolcarboxylic acid

There total 22 articles about 2-[(1R)-1-({[(6R)-6-(5-Chloro-2-methoxybenzyl)-3,7-dioxo-1,4-diazepan-1-yl]carbonyl}amino)propyl]-4-oxazolcarboxylic acid 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:
Guidance literature:
Multi-step reaction with 6 steps
1.1: diethylamino-sulfur trifluoride / dichloromethane / 1 h / -20 °C
1.2: 6 h / 0 °C
2.1: sodium hydroxide; water / methanol / 3 h / 20 °C
3.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / dichloromethane / 2.5 h / 20 °C
4.1: hydrogenchloride / ethyl acetate / 2 h / 20 °C
5.1: dmap; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 15 h / 0 °C
6.1: acetic acid; zinc / 3 h / 20 °C
With hydrogenchloride; dmap; diethylamino-sulfur trifluoride; water; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; sodium hydroxide; zinc; In methanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2013.04.079
Guidance literature:
Multi-step reaction with 5 steps
1: sodium hydroxide; water / methanol / 3 h / 20 °C
2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / dichloromethane / 2.5 h / 20 °C
3: hydrogenchloride / ethyl acetate / 2 h / 20 °C
4: dmap; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 15 h / 0 °C
5: acetic acid; zinc / 3 h / 20 °C
With hydrogenchloride; dmap; water; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; sodium hydroxide; zinc; In methanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2013.04.079
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