Technology Process of C66H105N5O17Si
There total 11 articles about C66H105N5O17Si which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 8 steps
1.1: 78 percent / Et3N; DMAP; isopropenyl chloroformate / CH2Cl2 / 1.5 h / 0 °C
2.1: H2 / Pd/C / methanol; ethyl acetate / 5 h / 2585.81 Torr
3.1: BOP-Cl; NMM / CH2Cl2 / 0.75 h / -15 - 0 °C
3.2: 2.90 g / NMM / CH2Cl2 / 6 h / 0 °C
4.1: MgBr2 / CH2Cl2 / 3 h / 0 °C
5.1: 63 percent / HATU; DIEA / CH2Cl2 / 14 h / 0 - 20 °C
6.1: 75 percent / aq. AcOH / tetrahydrofuran / 24 h / 20 °C
7.1: Dess-Martin periodinane / CH2Cl2
8.1: 0.504 g / NaOCl2; aq. H2PO4*H2O / dimethylsulfoxide; acetonitrile / 16 h
With
4-methyl-morpholine; dmap; Isopropenyl chloroformate; hydrogen; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; dihydrogen phosphate; Dess-Martin periodane; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; magnesium bromide;
palladium on activated charcoal;
In
tetrahydrofuran; methanol; dichloromethane; dimethyl sulfoxide; ethyl acetate; acetonitrile;
7.1: Dess-Martin oxidation;
DOI:10.1021/jo0105991
- Guidance literature:
-
Multi-step reaction with 8 steps
1.1: 78 percent / Et3N; DMAP; isopropenyl chloroformate / CH2Cl2 / 1.5 h / 0 °C
2.1: H2 / Pd/C / methanol; ethyl acetate / 5 h / 2585.81 Torr
3.1: BOP-Cl; NMM / CH2Cl2 / 0.75 h / -15 - 0 °C
3.2: 2.90 g / NMM / CH2Cl2 / 6 h / 0 °C
4.1: MgBr2 / CH2Cl2 / 3 h / 0 °C
5.1: 63 percent / HATU; DIEA / CH2Cl2 / 14 h / 0 - 20 °C
6.1: 75 percent / aq. AcOH / tetrahydrofuran / 24 h / 20 °C
7.1: Dess-Martin periodinane / CH2Cl2
8.1: 0.504 g / NaOCl2; aq. H2PO4*H2O / dimethylsulfoxide; acetonitrile / 16 h
With
4-methyl-morpholine; dmap; Isopropenyl chloroformate; hydrogen; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; dihydrogen phosphate; Dess-Martin periodane; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; magnesium bromide;
palladium on activated charcoal;
In
tetrahydrofuran; methanol; dichloromethane; dimethyl sulfoxide; ethyl acetate; acetonitrile;
7.1: Dess-Martin oxidation;
DOI:10.1021/jo0105991
- Guidance literature:
-
Multi-step reaction with 9 steps
1.1: 97 percent / LiOH*H2O / tetrahydrofuran; methanol / 18 h / 0 - 20 °C
2.1: 78 percent / Et3N; DMAP; isopropenyl chloroformate / CH2Cl2 / 1.5 h / 0 °C
3.1: H2 / Pd/C / methanol; ethyl acetate / 5 h / 2585.81 Torr
4.1: BOP-Cl; NMM / CH2Cl2 / 0.75 h / -15 - 0 °C
4.2: 2.90 g / NMM / CH2Cl2 / 6 h / 0 °C
5.1: MgBr2 / CH2Cl2 / 3 h / 0 °C
6.1: 63 percent / HATU; DIEA / CH2Cl2 / 14 h / 0 - 20 °C
7.1: 75 percent / aq. AcOH / tetrahydrofuran / 24 h / 20 °C
8.1: Dess-Martin periodinane / CH2Cl2
9.1: 0.504 g / NaOCl2; aq. H2PO4*H2O / dimethylsulfoxide; acetonitrile / 16 h
With
4-methyl-morpholine; dmap; lithium hydroxide; Isopropenyl chloroformate; hydrogen; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; dihydrogen phosphate; Dess-Martin periodane; acetic acid; triethylamine; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; magnesium bromide;
palladium on activated charcoal;
In
tetrahydrofuran; methanol; dichloromethane; dimethyl sulfoxide; ethyl acetate; acetonitrile;
8.1: Dess-Martin oxidation;
DOI:10.1021/jo0105991