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cystodytin-N14-2-phenylacetamide

Base Information
  • Chemical Name:cystodytin-N14-2-phenylacetamide
  • CAS No.:1430088-70-2
  • Molecular Formula:C25H19N3O2
  • Molecular Weight:393.445
  • Hs Code.:
cystodytin-N<SUP>14</SUP>-2-phenylacetamide

Synonyms:

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Chemical Property of cystodytin-N14-2-phenylacetamide
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Technology Process of cystodytin-N14-2-phenylacetamide

There total 8 articles about cystodytin-N14-2-phenylacetamide 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:
With sodium hydrogencarbonate; silver(l) oxide; In methanol;
DOI:10.3390/md11020274
Guidance literature:
Multi-step reaction with 4 steps
1.1: triethylamine; PyBOP / N,N-dimethyl-formamide / 20 h / 20 °C / Inert atmosphere
2.1: boron tribromide / dichloromethane / 20 h / 0 - 20 °C
3.1: cerium(III) chloride heptahydrate; silver(l) oxide / acetic acid; methanol / 1.5 h / 40 °C / Inert atmosphere
3.2: 0.5 h / 90 °C
4.1: silver(l) oxide; sodium hydrogencarbonate / methanol
With cerium(III) chloride heptahydrate; PyBOP; boron tribromide; sodium hydrogencarbonate; triethylamine; silver(l) oxide; In methanol; dichloromethane; acetic acid; N,N-dimethyl-formamide;
DOI:10.3390/md11020274
Guidance literature:
Multi-step reaction with 3 steps
1.1: boron tribromide / dichloromethane / 20 h / 0 - 20 °C
2.1: cerium(III) chloride heptahydrate; silver(l) oxide / acetic acid; methanol / 1.5 h / 40 °C / Inert atmosphere
2.2: 0.5 h / 90 °C
3.1: silver(l) oxide; sodium hydrogencarbonate / methanol
With cerium(III) chloride heptahydrate; boron tribromide; sodium hydrogencarbonate; silver(l) oxide; In methanol; dichloromethane; acetic acid;
DOI:10.3390/md11020274
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