Acetic acid 2-[tert-butoxycarbonyl-((3Z,6Z)-(R)-11-oxo-1-propyl-undeca-3,6-dienyl)-amino]-ethyl ester

Base Information

Chemical Name:Acetic acid 2-[tert-butoxycarbonyl-((3Z,6Z)-(R)-11-oxo-1-propyl-undeca-3,6-dienyl)-amino]-ethyl ester
CAS No.:185418-85-3
Molecular Formula:C₂₃H₃₉NO₅
Molecular Weight:409.566
Hs Code.:

Synonyms:Acetic acid 2-[tert-butoxycarbonyl-((3Z,6Z)-(R)-11-oxo-1-propyl-undeca-3,6-dienyl)-amino]-ethyl ester

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Chemical Property of Acetic acid 2-[tert-butoxycarbonyl-((3Z,6Z)-(R)-11-oxo-1-propyl-undeca-3,6-dienyl)-amino]-ethyl ester

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Technology Process of Acetic acid 2-[tert-butoxycarbonyl-((3Z,6Z)-(R)-11-oxo-1-propyl-undeca-3,6-dienyl)-amino]-ethyl ester

There total 1 articles about Acetic acid 2-[tert-butoxycarbonyl-((3Z,6Z)-(R)-11-oxo-1-propyl-undeca-3,6-dienyl)-amino]-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:

Reference yield:

: 89321-71-1
(2S,3S)-3-propyl-2-oxiranemethanol

: 185418-85-3
Acetic acid 2-[tert-butoxycarbonyl-((3Z,6Z)-(R)-11-oxo-1-propyl-undeca-3,6-dienyl)-amino]-ethyl ester

Guidance literature:: Multi-step reaction with 11 steps

1: 72 percent / PPh₃, CCl₄, NaHCO₃ / 3 h / Heating

2: 70 percent / LiNH₂ / tetrahydrofuran / 6 h / -30 °C

3: 65 percent / NaNH₂, diaminopropane / 2 h / 80 °C

4: 1.) EtMgBr, 2.) CuCl / 1.) THF, 2.) THF

5: 86 percent / H₂ / Pd/CaCO₃ / methanol / 3 h

6: NEt₃ / CH₂Cl₂ / 3 h / 0 °C

7: 8 h / 80 °C

8: 75 percent / NEt₃ / CH₂Cl₂ / 3 h / Ambient temperature

9: 95 percent / DMAP / CH₂Cl₂ / 1 h / Ambient temperature

10: 82 percent / PPTS / ethanol / 4 h / Heating

11: PCC, celite / CH₂Cl₂ / 3 h

With tetrachloromethane; dmap; lithium amide; Celite; ethylmagnesium bromide; hydrogen; pyridinium p-toluenesulfonate; sodium hydrogencarbonate; sodium amide; Trimethylenediamine; triethylamine; triphenylphosphine; pyridinium chlorochromate; copper(l) chloride; Lindlar's catalyst; In tetrahydrofuran; methanol; ethanol; dichloromethane;
DOI:10.1016/0040-4039(96)01960-0

Reference yield:

: 185418-85-3
Acetic acid 2-[tert-butoxycarbonyl-((3Z,6Z)-(R)-11-oxo-1-propyl-undeca-3,6-dienyl)-amino]-ethyl ester

: C₃₅H₃₉Cl₆NO₇

Guidance literature:: Multi-step reaction with 2 steps

1: Ag₂O, NaOH, H₂O / ethanol / 4 h / Ambient temperature

2: NEt₃ / tetrahydrofuran / 2 h / Ambient temperature

With sodium hydroxide; water; triethylamine; silver(l) oxide; In tetrahydrofuran; ethanol;
DOI:10.1016/0040-4039(96)01960-0

Reference yield:

: 185418-85-3
Acetic acid 2-[tert-butoxycarbonyl-((3Z,6Z)-(R)-11-oxo-1-propyl-undeca-3,6-dienyl)-amino]-ethyl ester

: 147363-83-5
(7Z,10Z)-(R)-5-Propyl-1-oxa-4-aza-cyclopentadeca-7,10-dien-15-one

Guidance literature:: Multi-step reaction with 4 steps

1: Ag₂O, NaOH, H₂O / ethanol / 4 h / Ambient temperature

2: NEt₃ / tetrahydrofuran / 2 h / Ambient temperature

3: 78 percent / DMAP / toluene / 12 h / 90 °C

4: 90 percent / TFA / 0.25 h / Ambient temperature

With dmap; sodium hydroxide; water; triethylamine; trifluoroacetic acid; silver(l) oxide; In tetrahydrofuran; ethanol; toluene;
DOI:10.1016/0040-4039(96)01960-0