1-{(1R,3R,4S)-3-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-cyclopentyl}-5-methyl-1H-pyrimidine-2,4-dione

Base Information

Chemical Name:1-{(1R,3R,4S)-3-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-cyclopentyl}-5-methyl-1H-pyrimidine-2,4-dione
CAS No.:127526-25-4
Molecular Formula:C₃₂H₃₄N₂O₆
Molecular Weight:542.632
Hs Code.:

Synonyms:1-{(1R,3R,4S)-3-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-cyclopentyl}-5-methyl-1H-pyrimidine-2,4-dione

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Chemical Property of 1-{(1R,3R,4S)-3-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-cyclopentyl}-5-methyl-1H-pyrimidine-2,4-dione

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Technology Process of 1-{(1R,3R,4S)-3-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-cyclopentyl}-5-methyl-1H-pyrimidine-2,4-dione

There total 9 articles about 1-{(1R,3R,4S)-3-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-cyclopentyl}-5-methyl-1H-pyrimidine-2,4-dione 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: 65.0%

: 40615-36-9
4,4'-dimethoxytrityl chloride

: 114884-15-0
1-((1R,3S,4R)-3-hydroxy-4-(hydroxymethyl)cyclopentyl)-5-methylpyrimidine-2,4(1H,3H)-dione

: 127526-25-4
1-{(1R,3R,4S)-3-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-cyclopentyl}-5-methyl-1H-pyrimidine-2,4-dione

Guidance literature:: With pyridine;
DOI:10.1016/S0040-4039(99)01113-2

Reference yield:

: 162427-15-8
3-oxo-2-aza-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid tert-butyl ester

: 127526-25-4
1-{(1R,3R,4S)-3-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-cyclopentyl}-5-methyl-1H-pyrimidine-2,4-dione

Guidance literature:: Multi-step reaction with 8 steps

1: oxone; KOH

2: 89 percent / NaBH₄ / methanol / 0 °C

3: 97 percent / 2,6-lutidine / CH₂Cl₂

4: 85 percent / Red-Al / toluene

5: H₂O / Heating

6: 75 percent / DMF*Et₂O

7: 83 percent / NH₃ / Heating

8: 65 percent / pyridine

With pyridine; 2,6-dimethylpyridine; Oxone; potassium hydroxide; sodium tetrahydroborate; ammonia; water; N,N-dimethyl-formamide; sodium bis(2-methoxyethoxy)aluminium dihydride; In methanol; dichloromethane; toluene; 1: Epoxidation / 2: Reduction / 3: Etherification / 4: Reduction / 5: Hydrolysis / 6: Addition / 7: Cyclization / 8: Etherification;
DOI:10.1016/S0040-4039(99)01113-2

Reference yield:

: 244057-71-4
tert-butyl N-[(1S,2R,4R,5R)-4-(hydroxymethyl)-6-oxabicyclo[3.1.0]hexan-2-yl]carbamate

: 127526-25-4
1-{(1R,3R,4S)-3-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-cyclopentyl}-5-methyl-1H-pyrimidine-2,4-dione

Guidance literature:: Multi-step reaction with 6 steps

1: 97 percent / 2,6-lutidine / CH₂Cl₂

2: 85 percent / Red-Al / toluene

3: H₂O / Heating

4: 75 percent / DMF*Et₂O

5: 83 percent / NH₃ / Heating

6: 65 percent / pyridine

With pyridine; 2,6-dimethylpyridine; ammonia; water; N,N-dimethyl-formamide; sodium bis(2-methoxyethoxy)aluminium dihydride; In dichloromethane; toluene; 1: Etherification / 2: Reduction / 3: Hydrolysis / 4: Addition / 5: Cyclization / 6: Etherification;
DOI:10.1016/S0040-4039(99)01113-2