N-allyl-N-((S)-1-(2-((1S,2S)-3-(allyloxy)-1,2-dimethoxypropyl)phenylamino)-1-oxo-3-phenylpropan-2-yl)-4-fluorobenzamide

Base Information

Chemical Name:N-allyl-N-((S)-1-(2-((1S,2S)-3-(allyloxy)-1,2-dimethoxypropyl)phenylamino)-1-oxo-3-phenylpropan-2-yl)-4-fluorobenzamide
CAS No.:1421051-55-9
Molecular Formula:C₃₃H₃₇FN₂O₅
Molecular Weight:560.666
Hs Code.:

Synonyms:N-allyl-N-((S)-1-(2-((1S,2S)-3-(allyloxy)-1,2-dimethoxypropyl)phenylamino)-1-oxo-3-phenylpropan-2-yl)-4-fluorobenzamide

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Chemical Property of N-allyl-N-((S)-1-(2-((1S,2S)-3-(allyloxy)-1,2-dimethoxypropyl)phenylamino)-1-oxo-3-phenylpropan-2-yl)-4-fluorobenzamide

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Technology Process of N-allyl-N-((S)-1-(2-((1S,2S)-3-(allyloxy)-1,2-dimethoxypropyl)phenylamino)-1-oxo-3-phenylpropan-2-yl)-4-fluorobenzamide

There total 5 articles about N-allyl-N-((S)-1-(2-((1S,2S)-3-(allyloxy)-1,2-dimethoxypropyl)phenylamino)-1-oxo-3-phenylpropan-2-yl)-4-fluorobenzamide 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: 85.6%

: 1421051-47-9
(S)-2-(allylamino)-N-(2-((1S,2S)-3-(allyloxy)-1,2-dimethoxypropyl)phenyl)-3-phenylpropanamide

: 403-43-0
4-fluorobenzoyl chloride

: 1421051-55-9
N-allyl-N-((S)-1-(2-((1S,2S)-3-(allyloxy)-1,2-dimethoxypropyl)phenylamino)-1-oxo-3-phenylpropan-2-yl)-4-fluorobenzamide

Guidance literature:: In dichloromethane; at 0 - 20 ℃; for 0.0833333h;
DOI:10.1021/ol3032126

Reference yield:

: 1421051-40-2
C₂₃H₃₀N₂O₄

: 1421051-55-9
N-allyl-N-((S)-1-(2-((1S,2S)-3-(allyloxy)-1,2-dimethoxypropyl)phenylamino)-1-oxo-3-phenylpropan-2-yl)-4-fluorobenzamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / methanol / 12 h / Reflux

2: dichloromethane / 0.08 h / 0 - 20 °C

With triethylamine; In methanol; dichloromethane;
DOI:10.1021/ol3032126

Reference yield:

: C₁₄H₁₉NO₅

: 1421051-55-9
N-allyl-N-((S)-1-(2-((1S,2S)-3-(allyloxy)-1,2-dimethoxypropyl)phenylamino)-1-oxo-3-phenylpropan-2-yl)-4-fluorobenzamide

Guidance literature:: Multi-step reaction with 5 steps

1: acetic acid; zinc / ethanol / 0.5 h / 0 - 20 °C

2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / acetonitrile / 3 h / 20 °C

3: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 0.08 h / 20 °C

4: triethylamine / methanol / 12 h / Reflux

5: dichloromethane / 0.08 h / 0 - 20 °C

With acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; zinc; In tetrahydrofuran; methanol; ethanol; dichloromethane; acetonitrile;
DOI:10.1021/ol3032126