Technology Process of 2-[2-fluoro-3-(4-methoxy-benzyl)-5-nitro-benzylamino]-ethanol
There total 11 articles about 2-[2-fluoro-3-(4-methoxy-benzyl)-5-nitro-benzylamino]-ethanol which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
sodium cyanoborohydride; acetic acid;
In
methanol;
for 3h;
Heating;
DOI:10.1021/jm051222g
- Guidance literature:
-
Multi-step reaction with 9 steps
1: 58 percent / KMnO4; KOH / H2O / Heating
2: 40 percent / H2SO4 / 48 h / 20 °C
3: 99 percent / HNO3; H2SO4 / 2 h / 20 °C
4: SOCl2 / 3 h / Heating
5: 3.24 g / AlCl3 / 20 h / 20 °C
6: 98 percent / TFA; trifluoromethanesulfonic acid; Et3SiH / CH2Cl2 / 6 h / 50 °C
7: 61 percent / NaBH4 / dioxane; H2O / 20 °C
8: 99 percent / (COCl)2; DMSO; Et3N / CH2Cl2 / -78 - -30 °C
9: 75 percent / NaCNBH3; AcOH / methanol / 3 h / Heating
With
triethylsilane; potassium hydroxide; sodium tetrahydroborate; potassium permanganate; aluminium trichloride; thionyl chloride; oxalyl dichloride; trifluorormethanesulfonic acid; sulfuric acid; nitric acid; sodium cyanoborohydride; acetic acid; dimethyl sulfoxide; triethylamine; trifluoroacetic acid;
In
1,4-dioxane; methanol; dichloromethane; water;
5: Friedel-Crafts acylation / 8: Swern oxidation;
DOI:10.1021/jm051222g
- Guidance literature:
-
Multi-step reaction with 8 steps
1: 40 percent / H2SO4 / 48 h / 20 °C
2: 99 percent / HNO3; H2SO4 / 2 h / 20 °C
3: SOCl2 / 3 h / Heating
4: 3.24 g / AlCl3 / 20 h / 20 °C
5: 98 percent / TFA; trifluoromethanesulfonic acid; Et3SiH / CH2Cl2 / 6 h / 50 °C
6: 61 percent / NaBH4 / dioxane; H2O / 20 °C
7: 99 percent / (COCl)2; DMSO; Et3N / CH2Cl2 / -78 - -30 °C
8: 75 percent / NaCNBH3; AcOH / methanol / 3 h / Heating
With
triethylsilane; sodium tetrahydroborate; aluminium trichloride; thionyl chloride; oxalyl dichloride; trifluorormethanesulfonic acid; sulfuric acid; nitric acid; sodium cyanoborohydride; acetic acid; dimethyl sulfoxide; triethylamine; trifluoroacetic acid;
In
1,4-dioxane; methanol; dichloromethane; water;
4: Friedel-Crafts acylation / 7: Swern oxidation;
DOI:10.1021/jm051222g