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L-3,5-diiodo-4-(4'-methoxy-3'-(6-methoxy-3-pyridylmethyl)-phenylthio)-N-trifluoracetyl phenylalanine ethyl ester

Base Information
  • Chemical Name:L-3,5-diiodo-4-(4'-methoxy-3'-(6-methoxy-3-pyridylmethyl)-phenylthio)-N-trifluoracetyl phenylalanine ethyl ester
  • CAS No.:105189-65-9
  • Molecular Formula:C27H25F3I2N2O5S
  • Molecular Weight:800.376
  • Hs Code.:
L-3,5-diiodo-4-(4'-methoxy-3'-(6-methoxy-3-pyridylmethyl)-phenylthio)-N-trifluoracetyl phenylalanine ethyl ester

Synonyms:L-3,5-diiodo-4-(4'-methoxy-3'-(6-methoxy-3-pyridylmethyl)-phenylthio)-N-trifluoracetyl phenylalanine ethyl ester

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Chemical Property of L-3,5-diiodo-4-(4'-methoxy-3'-(6-methoxy-3-pyridylmethyl)-phenylthio)-N-trifluoracetyl phenylalanine ethyl ester
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Technology Process of L-3,5-diiodo-4-(4'-methoxy-3'-(6-methoxy-3-pyridylmethyl)-phenylthio)-N-trifluoracetyl phenylalanine ethyl ester

There total 12 articles about L-3,5-diiodo-4-(4'-methoxy-3'-(6-methoxy-3-pyridylmethyl)-phenylthio)-N-trifluoracetyl phenylalanine ethyl ester 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 8 steps
1: 1) n-BuLi / 1) THF, hexane, -85 deg C, 5 min, 2) THF, below -70 deg C to room temperature
2: pyridine / 50 °C
3: H2 / 10percent Pd/C / methanol
4: 55 percent / Ac2O, Cl2 / acetic acid / 20 h / Ambient temperature
5: 2.55 g / NaOH / dioxane; H2O / 5 h / Heating
6: 1) Me2SO2Cl, pyridine, 2) pyridine / 1) reflux, 10 min, 2) reflux, 20 min
7: H2 / 10percent Pd/C / acetic acid
8: 1) NaNO2, H2SO4, 2) KI, I2
With pyridine; sodium hydroxide; n-butyllithium; Me2SO2Cl; sulfuric acid; hydrogen; iodine; acetic anhydride; chlorine; potassium iodide; sodium nitrite; palladium on activated charcoal; In 1,4-dioxane; methanol; water; acetic acid;
DOI:10.1021/jm00122a009
Guidance literature:
Multi-step reaction with 8 steps
1: 1) n-BuLi / 1) THF, hexane, -85 deg C, 5 min, 2) THF, below -70 deg C to room temperature
2: pyridine / 50 °C
3: H2 / 10percent Pd/C / methanol
4: 55 percent / Ac2O, Cl2 / acetic acid / 20 h / Ambient temperature
5: 2.55 g / NaOH / dioxane; H2O / 5 h / Heating
6: 1) Me2SO2Cl, pyridine, 2) pyridine / 1) reflux, 10 min, 2) reflux, 20 min
7: H2 / 10percent Pd/C / acetic acid
8: 1) NaNO2, H2SO4, 2) KI, I2
With pyridine; sodium hydroxide; n-butyllithium; Me2SO2Cl; sulfuric acid; hydrogen; iodine; acetic anhydride; chlorine; potassium iodide; sodium nitrite; palladium on activated charcoal; In 1,4-dioxane; methanol; water; acetic acid;
DOI:10.1021/jm00122a009
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