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(2R,4R,5S)-5-(3,5-Dibenzyl-4-oxo-[1,3,5]triazinan-1-yl)-4-hydroxy-2-tridecyl-piperidine-1-carboxylic acid tert-butyl ester

Base Information
  • Chemical Name:(2R,4R,5S)-5-(3,5-Dibenzyl-4-oxo-[1,3,5]triazinan-1-yl)-4-hydroxy-2-tridecyl-piperidine-1-carboxylic acid tert-butyl ester
  • CAS No.:1054667-53-6
  • Molecular Formula:C40H62N4O4
  • Molecular Weight:662.957
  • Hs Code.:
(2R,4R,5S)-5-(3,5-Dibenzyl-4-oxo-[1,3,5]triazinan-1-yl)-4-hydroxy-2-tridecyl-piperidine-1-carboxylic acid tert-butyl ester

Synonyms:(2R,4R,5S)-5-(3,5-Dibenzyl-4-oxo-[1,3,5]triazinan-1-yl)-4-hydroxy-2-tridecyl-piperidine-1-carboxylic acid tert-butyl ester

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Chemical Property of (2R,4R,5S)-5-(3,5-Dibenzyl-4-oxo-[1,3,5]triazinan-1-yl)-4-hydroxy-2-tridecyl-piperidine-1-carboxylic acid tert-butyl ester
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Technology Process of (2R,4R,5S)-5-(3,5-Dibenzyl-4-oxo-[1,3,5]triazinan-1-yl)-4-hydroxy-2-tridecyl-piperidine-1-carboxylic acid tert-butyl ester

There total 19 articles about (2R,4R,5S)-5-(3,5-Dibenzyl-4-oxo-[1,3,5]triazinan-1-yl)-4-hydroxy-2-tridecyl-piperidine-1-carboxylic acid tert-butyl ester 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:
Guidance literature:
Multi-step reaction with 6 steps
1: DIPEA / CH2Cl2
2: LiBH4 / tetrahydrofuran / Heating
3: (COCl)2, DMSO, DIPEA / CH2Cl2
5: H2 / 10percent Pd-C / ethanol
6: tetra-n-butylammonium fluoride / tetrahydrofuran
With lithium borohydride; oxalyl dichloride; tetrabutyl ammonium fluoride; hydrogen; dimethyl sulfoxide; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1021/jo00062a003
Guidance literature:
Multi-step reaction with 19 steps
1: 2) ethyl acetate, reflux
2: LiBH4 / diethyl ether
3: Zn(N3)2(py)2, Ph3P, DEAD, imid / toluene
4: H2 / 10percent Pd/C / ethanol
5: pyridine / CH2Cl2
6: TBAF / tetrahydrofuran / 0 to 25 deg C
7: (COCl)2, DMSO, DIPEA / CH2Cl2
8: BF3*Et2O / CH2Cl2 / -78 - -20 °C
9: DIPEA / CH2Cl2 / 0 °C
10: OsO4, NMO / acetone; butan-1-ol; H2O
11: NaIO4 / tetrahydrofuran; H2O
12: toluene / 70 °C
13: 85 percent / 8.8 eq. NaBH4 / methanol
14: DIPEA / CH2Cl2
15: LiBH4 / tetrahydrofuran / Heating
16: (COCl)2, DMSO, DIPEA / CH2Cl2
18: H2 / 10percent Pd-C / ethanol
19: tetra-n-butylammonium fluoride / tetrahydrofuran
With pyridine; 1H-imidazole; sodium tetrahydroborate; sodium periodate; osmium(VIII) oxide; lithium borohydride; N-methyl-2-indolinone; oxalyl dichloride; Zn(N3)2/bis-pyridine complex; boron trifluoride diethyl etherate; tetrabutyl ammonium fluoride; hydrogen; dimethyl sulfoxide; N-ethyl-N,N-diisopropylamine; triphenylphosphine; diethylazodicarboxylate; palladium on activated charcoal; In tetrahydrofuran; methanol; diethyl ether; ethanol; dichloromethane; water; acetone; toluene; butan-1-ol;
DOI:10.1021/jo00062a003
Guidance literature:
Multi-step reaction with 15 steps
1: pyridine / CH2Cl2
2: TBAF / tetrahydrofuran / 0 to 25 deg C
3: (COCl)2, DMSO, DIPEA / CH2Cl2
4: BF3*Et2O / CH2Cl2 / -78 - -20 °C
5: DIPEA / CH2Cl2 / 0 °C
6: OsO4, NMO / acetone; butan-1-ol; H2O
7: NaIO4 / tetrahydrofuran; H2O
8: toluene / 70 °C
9: 85 percent / 8.8 eq. NaBH4 / methanol
10: DIPEA / CH2Cl2
11: LiBH4 / tetrahydrofuran / Heating
12: (COCl)2, DMSO, DIPEA / CH2Cl2
14: H2 / 10percent Pd-C / ethanol
15: tetra-n-butylammonium fluoride / tetrahydrofuran
With pyridine; sodium tetrahydroborate; sodium periodate; osmium(VIII) oxide; lithium borohydride; N-methyl-2-indolinone; oxalyl dichloride; boron trifluoride diethyl etherate; tetrabutyl ammonium fluoride; hydrogen; dimethyl sulfoxide; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; acetone; toluene; butan-1-ol;
DOI:10.1021/jo00062a003
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