Technology Process of (1R)-3-{(1R)-3-[(9H-fluoren-9-yl)methoxy]-1-methyl-3-oxopropoxy}-1-methyl-3-oxopropyl (4R,8R,22R,26R)-31-({[(tert-butyl)diphenylsilyl]oxy}methyl)-4,8,22,26-tetramethyl-2,6,10,20,24,28-hexaoxo-3,7,11,19,23,27-hexaoxatricyclo[27.3.1.113.17]tetratriac...
There total 18 articles about (1R)-3-{(1R)-3-[(9H-fluoren-9-yl)methoxy]-1-methyl-3-oxopropoxy}-1-methyl-3-oxopropyl (4R,8R,22R,26R)-31-({[(tert-butyl)diphenylsilyl]oxy}methyl)-4,8,22,26-tetramethyl-2,6,10,20,24,28-hexaoxo-3,7,11,19,23,27-hexaoxatricyclo[27.3.1.113.17]tetratriac... 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:
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193953-35-4
(1R)-3-{(1R)-3-[(9H-fluoren-9-yl)methoxy]-1-methyl-3-oxopropoxy}-1-methyl-3-oxopropyl (4R,8R,22R,26R)-31-({[(tert-butyl)diphenylsilyl]oxy}methyl)-4,8,22,26-tetramethyl-2,6,10,20,24,28-hexaoxo-3,7,11,19,23,27-hexaoxatricyclo[27.3.1.113.17]tetratriac...
- Guidance literature:
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Multi-step reaction with 8 steps
1: 23 percent / LiAlH4 / tetrahydrofuran / 0.17 h / 1 - 30 °C
2: KOH / methanol
3: (i-Pr)2NH / dimethylformamide / 24 h / Ambient temperature
4: 81 percent / 1 N KOH / ethanol; H2O / 0.33 h / Ambient temperature
5: oxalyl chloride / CH2Cl2; dimethylformamide / Ambient temperature
6: pyridine / CH2Cl2 / 0 °C / to RT
7: 98 percent / HF*pyridine / CH2Cl2 / 0.25 h / 0 °C
8: pyridine / CH2Cl2 / -78 deg C, 5 h, RT, 36 h
With
pyridine; potassium hydroxide; lithium aluminium tetrahydride; oxalyl dichloride; pyridine hydrogenfluoride; diisopropylamine;
In
tetrahydrofuran; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1002/hlca.19970800402
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193953-35-4
(1R)-3-{(1R)-3-[(9H-fluoren-9-yl)methoxy]-1-methyl-3-oxopropoxy}-1-methyl-3-oxopropyl (4R,8R,22R,26R)-31-({[(tert-butyl)diphenylsilyl]oxy}methyl)-4,8,22,26-tetramethyl-2,6,10,20,24,28-hexaoxo-3,7,11,19,23,27-hexaoxatricyclo[27.3.1.113.17]tetratriac...
- Guidance literature:
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Multi-step reaction with 7 steps
1: 92.8 percent / DMAP / dimethylformamide / 24 h / Ambient temperature
2: 78 percent / LiOH / methanol; dioxane; H2O / 0.5 h
3: (COCl)2 / dimethylformamide / 14 h
4: pyridine, (t-Bu)Ph2SiF / CH2Cl2 / 0 deg C, 3 h, RT, 8 h
5: 98 percent / H2 / 10 percent Pd/C / various solvent(s)
6: oxalyl chloride / CH2Cl2 / Ambient temperature
7: pyridine / CH2Cl2 / -78 deg C, 5 h, RT, 36 h
With
pyridine; dmap; lithium hydroxide; oxalyl dichloride; hydrogen; tert-butyl diphenylfluorosilane;
palladium on activated charcoal;
In
1,4-dioxane; methanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1002/hlca.19970800402
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193953-35-4
(1R)-3-{(1R)-3-[(9H-fluoren-9-yl)methoxy]-1-methyl-3-oxopropoxy}-1-methyl-3-oxopropyl (4R,8R,22R,26R)-31-({[(tert-butyl)diphenylsilyl]oxy}methyl)-4,8,22,26-tetramethyl-2,6,10,20,24,28-hexaoxo-3,7,11,19,23,27-hexaoxatricyclo[27.3.1.113.17]tetratriac...
- Guidance literature:
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Multi-step reaction with 5 steps
1: (COCl)2 / dimethylformamide / 14 h
2: pyridine, (t-Bu)Ph2SiF / CH2Cl2 / 0 deg C, 3 h, RT, 8 h
3: 98 percent / H2 / 10 percent Pd/C / various solvent(s)
4: oxalyl chloride / CH2Cl2 / Ambient temperature
5: pyridine / CH2Cl2 / -78 deg C, 5 h, RT, 36 h
With
pyridine; oxalyl dichloride; hydrogen; tert-butyl diphenylfluorosilane;
palladium on activated charcoal;
In
dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/hlca.19970800402