N-1-[(1S,4R)-4-{(monomethoxytrityl)oxymethyl}cyclopentyl]-5'-O-(tert-butyldimethylsilyl)-2',3'-O-isopropylideneadenosine

Base Information

Chemical Name:N-1-[(1S,4R)-4-{(monomethoxytrityl)oxymethyl}cyclopentyl]-5'-O-(tert-butyldimethylsilyl)-2',3'-O-isopropylideneadenosine
CAS No.:859147-53-8
Molecular Formula:C₄₅H₅₇N₅O₆Si
Molecular Weight:792.063
Hs Code.:

Synonyms:N-1-[(1S,4R)-4-{(monomethoxytrityl)oxymethyl}cyclopentyl]-5'-O-(tert-butyldimethylsilyl)-2',3'-O-isopropylideneadenosine

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Chemical Property of N-1-[(1S,4R)-4-{(monomethoxytrityl)oxymethyl}cyclopentyl]-5'-O-(tert-butyldimethylsilyl)-2',3'-O-isopropylideneadenosine

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Technology Process of N-1-[(1S,4R)-4-{(monomethoxytrityl)oxymethyl}cyclopentyl]-5'-O-(tert-butyldimethylsilyl)-2',3'-O-isopropylideneadenosine

There total 7 articles about N-1-[(1S,4R)-4-{(monomethoxytrityl)oxymethyl}cyclopentyl]-5'-O-(tert-butyldimethylsilyl)-2',3'-O-isopropylideneadenosine 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: 97.0%

: 859147-51-6
N-1-{(1S,4R)-4-(hydroxymethyl)cyclopentyl}-5'-O-(tert-butyldimethylsilyl)-2',3'-O-isopropylideneadenosine

: 14470-28-1
mono-4-methoxytrityl chloride

: 859147-53-8
N-1-[(1S,4R)-4-{(monomethoxytrityl)oxymethyl}cyclopentyl]-5'-O-(tert-butyldimethylsilyl)-2',3'-O-isopropylideneadenosine

Guidance literature:: With pyridine; at 20 ℃; for 4h;
DOI:10.1021/ja050732x

Reference yield:

: 79200-56-9
(-)-2-azabicyclo[2.2.1]hept-5-en-3-one

: 859147-53-8
N-1-[(1S,4R)-4-{(monomethoxytrityl)oxymethyl}cyclopentyl]-5'-O-(tert-butyldimethylsilyl)-2',3'-O-isopropylideneadenosine

Guidance literature:: Multi-step reaction with 6 steps

1: 100 percent / H₂ / Pd-C / methanol / 5 h / 20 °C / atmospheric pressure

2: 100 percent / DMAP / acetonitrile / 1 h / 20 °C

3: 95 percent / NaBH₄ / methanol / 0.5 h / 0 °C

4: 100 percent / water / 18 h / Heating

5: 85 percent / K₂CO₃ / methanol / 14 h / 20 °C

6: 97 percent / pyridine / 4 h / 20 °C

With pyridine; dmap; sodium tetrahydroborate; water; hydrogen; potassium carbonate; palladium on activated charcoal; In methanol; acetonitrile;
DOI:10.1021/ja050732x

Reference yield:

: 117957-62-7,1110772-11-6
(1S,3R)-1-amino-3-(hydroxymethyl)cyclopentanone

: 859147-53-8
N-1-[(1S,4R)-4-{(monomethoxytrityl)oxymethyl}cyclopentyl]-5'-O-(tert-butyldimethylsilyl)-2',3'-O-isopropylideneadenosine

Guidance literature:: Multi-step reaction with 2 steps

1: K₂CO₃ / methanol

2: pyridine

With pyridine; potassium carbonate; In methanol;
DOI:10.1081/NCN-200060167