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

Base Information

Chemical Name:N-1-[(1S,4R)-4-{(monomethoxytrityl)oxymethyl}cyclopentyl]-2',3'-O-isopropylideneadenosine
CAS No.:859147-55-0
Molecular Formula:C₃₉H₄₃N₅O₆
Molecular Weight:677.8
Hs Code.:

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

Suppliers and Price of N-1-[(1S,4R)-4-{(monomethoxytrityl)oxymethyl}cyclopentyl]-2',3'-O-isopropylideneadenosine

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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

Chemical Property:

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

There total 8 articles about N-1-[(1S,4R)-4-{(monomethoxytrityl)oxymethyl}cyclopentyl]-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: 100.0%

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

: 859147-55-0
N-1-[(1S,4R)-4-{(monomethoxytrityl)oxymethyl}cyclopentyl]-2',3'-O-isopropylideneadenosine

Guidance literature:: With tetrabutyl ammonium fluoride; acetic acid; In tetrahydrofuran; at 20 ℃; for 1h;
DOI:10.1021/ja050732x

Reference yield:

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

: 859147-55-0
N-1-[(1S,4R)-4-{(monomethoxytrityl)oxymethyl}cyclopentyl]-2',3'-O-isopropylideneadenosine

Guidance literature:: Multi-step reaction with 7 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

7: 100 percent / TBAF; AcOH / tetrahydrofuran / 1 h / 20 °C

With pyridine; dmap; sodium tetrahydroborate; tetrabutyl ammonium fluoride; water; hydrogen; potassium carbonate; acetic acid; palladium on activated charcoal; In tetrahydrofuran; methanol; acetonitrile;
DOI:10.1021/ja050732x

Reference yield:

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

: 859147-55-0
N-1-[(1S,4R)-4-{(monomethoxytrityl)oxymethyl}cyclopentyl]-2',3'-O-isopropylideneadenosine

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine

2: tetrabutylammonium fluoride; acetic acid / tetrahydrofuran

With pyridine; tetrabutyl ammonium fluoride; acetic acid; In tetrahydrofuran;
DOI:10.1081/NCN-200060167