(+)-N6-triphenylphosphinimino-(4'α-iodo-2'α,3'α-O-isopropylidendioxycyclopent-1'β-yl)-9-H-adenine

Base Information

Chemical Name:(+)-N6-triphenylphosphinimino-(4'α-iodo-2'α,3'α-O-isopropylidendioxycyclopent-1'β-yl)-9-H-adenine
CAS No.:219635-80-0
Molecular Formula:C₃₁H₂₉IN₅O₂P
Molecular Weight:661.482
Hs Code.:

Synonyms:(+)-N6-triphenylphosphinimino-(4'α-iodo-2'α,3'α-O-isopropylidendioxycyclopent-1'β-yl)-9-H-adenine

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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 (+)-N6-triphenylphosphinimino-(4'α-iodo-2'α,3'α-O-isopropylidendioxycyclopent-1'β-yl)-9-H-adenine

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Technology Process of (+)-N6-triphenylphosphinimino-(4'α-iodo-2'α,3'α-O-isopropylidendioxycyclopent-1'β-yl)-9-H-adenine

There total 7 articles about (+)-N6-triphenylphosphinimino-(4'α-iodo-2'α,3'α-O-isopropylidendioxycyclopent-1'β-yl)-9-H-adenine 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: 76.0%

: 603-35-0
triphenylphosphine

: 153830-48-9
(-)-β-(4'β-hydroxy-2'α,3'α-O-isopropylidenedioxycyclopent-1'-yl)-9-H-adenine

: 219635-80-0
(+)-N6-triphenylphosphinimino-(4'α-iodo-2'α,3'α-O-isopropylidendioxycyclopent-1'β-yl)-9-H-adenine

Guidance literature:: With tri-iodoimidazole; In toluene; at 120 ℃; for 21h;
DOI:10.1080/07328319808004308

Reference yield:

: 60410-16-4
(1R,4S)-4-hydroxy-2-cyclopentene-1-yl acetate

: 219635-80-0
(+)-N6-triphenylphosphinimino-(4'α-iodo-2'α,3'α-O-isopropylidendioxycyclopent-1'β-yl)-9-H-adenine

Guidance literature:: Multi-step reaction with 6 steps

1: 55 percent / NaH, Pd(PPh₃)4 / dimethylformamide / 18 h / 60 °C

2: 85 percent / pyridine / 3 h / 65 °C

3: 90 percent / osmium tetroxide, trimethylamine N-oxide / dimethylformamide; acetone; H₂O / 15 h / Ambient temperature

4: 95 percent / p-TsOH*H₂O / 60 h / Ambient temperature

5: 75 percent / aq. NaOH / methanol / 12 h / Ambient temperature

6: 76 percent / triiodoimidazole / toluene / 21 h / 120 °C

With sodium hydroxide; osmium(VIII) oxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; trimethylamine-N-oxide; tri-iodoimidazole; sodium hydride; toluene-4-sulfonic acid; In pyridine; methanol; water; N,N-dimethyl-formamide; acetone; toluene;
DOI:10.1080/07328319808004308

Reference yield:

: 66224-66-6,66224-67-7,66224-68-8,66224-69-9,134434-48-3,134434-49-4,134454-76-5,134461-75-9
adenine

: 219635-80-0
(+)-N6-triphenylphosphinimino-(4'α-iodo-2'α,3'α-O-isopropylidendioxycyclopent-1'β-yl)-9-H-adenine

Guidance literature:: Multi-step reaction with 6 steps

1: 55 percent / NaH, Pd(PPh₃)4 / dimethylformamide / 18 h / 60 °C

2: 85 percent / pyridine / 3 h / 65 °C

3: 90 percent / osmium tetroxide, trimethylamine N-oxide / dimethylformamide; acetone; H₂O / 15 h / Ambient temperature

4: 95 percent / p-TsOH*H₂O / 60 h / Ambient temperature

5: 75 percent / aq. NaOH / methanol / 12 h / Ambient temperature

6: 76 percent / triiodoimidazole / toluene / 21 h / 120 °C

With sodium hydroxide; osmium(VIII) oxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; trimethylamine-N-oxide; tri-iodoimidazole; sodium hydride; toluene-4-sulfonic acid; In pyridine; methanol; water; N,N-dimethyl-formamide; acetone; toluene;
DOI:10.1080/07328319808004308