ethyl (-)-2-{(2R)-3-[(5-bromo-6-phenylfuro[2,3-d]pyrimidin-4-yl)oxy]-2-methylpropyloxy}acetate

Base Information

Chemical Name:ethyl (-)-2-{(2R)-3-[(5-bromo-6-phenylfuro[2,3-d]pyrimidin-4-yl)oxy]-2-methylpropyloxy}acetate
CAS No.:1093386-36-7
Molecular Formula:C₂₀H₂₁BrN₂O₅
Molecular Weight:449.301
Hs Code.:

Synonyms:ethyl (-)-2-{(2R)-3-[(5-bromo-6-phenylfuro[2,3-d]pyrimidin-4-yl)oxy]-2-methylpropyloxy}acetate

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Chemical Property of ethyl (-)-2-{(2R)-3-[(5-bromo-6-phenylfuro[2,3-d]pyrimidin-4-yl)oxy]-2-methylpropyloxy}acetate

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Technology Process of ethyl (-)-2-{(2R)-3-[(5-bromo-6-phenylfuro[2,3-d]pyrimidin-4-yl)oxy]-2-methylpropyloxy}acetate

There total 6 articles about ethyl (-)-2-{(2R)-3-[(5-bromo-6-phenylfuro[2,3-d]pyrimidin-4-yl)oxy]-2-methylpropyloxy}acetate 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: 15.5%

: 1073630-35-9
(-)-{[(2S)-3-hydroxy-2-methylpropyl]oxy}acetic acid ethyl ester

: 1073135-81-5
5-bromo-4-chloro-6-phenylfuro[2,3-d]pyrimidine

: 1093386-36-7
ethyl (-)-2-{(2R)-3-[(5-bromo-6-phenylfuro[2,3-d]pyrimidin-4-yl)oxy]-2-methylpropyloxy}acetate

Guidance literature:: With phosphazene base; In tetrahydrofuran; hexane; N,N-dimethyl-formamide; at -10 ℃; for 1h;

Reference yield:

: 1073630-34-8
(-)-{[(2R)-2-methyl-3-(trityloxy)propyl]oxy}acetic acid ethyl ester

: 1093386-36-7
ethyl (-)-2-{(2R)-3-[(5-bromo-6-phenylfuro[2,3-d]pyrimidin-4-yl)oxy]-2-methylpropyloxy}acetate

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogen / palladium 10% on activated carbon / ethanol / 3 h / 20 °C / 760.05 Torr

2: phosphazene base / N,N-dimethyl-formamide; hexane; tetrahydrofuran / 1 h / -10 °C

With hydrogen; palladium 10% on activated carbon; In tetrahydrofuran; ethanol; hexane; N,N-dimethyl-formamide;

Reference yield:

: 70-11-1
α-bromoacetophenone

: 1093386-36-7
ethyl (-)-2-{(2R)-3-[(5-bromo-6-phenylfuro[2,3-d]pyrimidin-4-yl)oxy]-2-methylpropyloxy}acetate

Guidance literature:: Multi-step reaction with 5 steps

1: diethylamine / N,N-dimethyl-formamide / 1 h / 20 °C

2: 1.5 h / 210 °C

3: N-Bromosuccinimide / tetrachloromethane / 60 °C

4: hydrogenchloride; isopentyl nitrite / 1,4-dioxane; chloroform / 3 h / Reflux

5: phosphazene base / N,N-dimethyl-formamide; hexane; tetrahydrofuran / 1 h / -10 °C

With hydrogenchloride; N-Bromosuccinimide; diethylamine; isopentyl nitrite; In tetrahydrofuran; 1,4-dioxane; tetrachloromethane; hexane; chloroform; N,N-dimethyl-formamide;