(2S)-benzyloxycarbonylamino-6-[N⁶-(2-methylpropionyl)-9-adeninyl]hexanoic acid

Base Information

Chemical Name:(2S)-benzyloxycarbonylamino-6-[N⁶-(2-methylpropionyl)-9-adeninyl]hexanoic acid
CAS No.:316353-30-7
Molecular Formula:C₂₃H₂₈N₆O₅
Molecular Weight:468.513
Hs Code.:

(2S)-benzyloxycarbonylamino-6-[N<sup>6</sup>-(2-methylpropionyl)-9-adeninyl]hexanoic acid

Synonyms:(2S)-benzyloxycarbonylamino-6-[N⁶-(2-methylpropionyl)-9-adeninyl]hexanoic acid

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Chemical Property of (2S)-benzyloxycarbonylamino-6-[N⁶-(2-methylpropionyl)-9-adeninyl]hexanoic acid

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Technology Process of (2S)-benzyloxycarbonylamino-6-[N⁶-(2-methylpropionyl)-9-adeninyl]hexanoic acid

There total 4 articles about (2S)-benzyloxycarbonylamino-6-[N⁶-(2-methylpropionyl)-9-adeninyl]hexanoic acid 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: 89.0%

: 316353-00-1
(2S,4S)-3-benzyloxycarbonyl-2-tert-butyl-4-{4-[N⁶-(2-methylpropionyl)-9-adeninyl]butyl}oxazolidin-5-one

: 316353-30-7
(2S)-benzyloxycarbonylamino-6-[N⁶-(2-methylpropionyl)-9-adeninyl]hexanoic acid

Guidance literature:: With lithium hydroxide; In tetrahydrofuran; water; at 0 ℃; for 1h;
DOI:10.1016/S0040-4020(01)00546-4

Reference yield:

: 109153-46-0
N⁶-(2-methylpropionyl)adenine

: 316353-30-7
(2S)-benzyloxycarbonylamino-6-[N⁶-(2-methylpropionyl)-9-adeninyl]hexanoic acid

Guidance literature:: Multi-step reaction with 4 steps

1: 76 percent / Ph₃P; i-PrO₂CN=NCO₂i-Pr / dioxane / 0 - 20 °C

2: 81 percent / NaI / acetone / Heating

3: 23 percent / AIBN; Bu₃SnH / toluene / 14 h / 80 °C

4: 89 percent / LiOH*H₂O / tetrahydrofuran; H₂O / 1 h / 0 °C

With lithium hydroxide; 2,2'-azobis(isobutyronitrile); di-isopropyl azodicarboxylate; tri-n-butyl-tin hydride; triphenylphosphine; sodium iodide; In tetrahydrofuran; 1,4-dioxane; water; acetone; toluene; 1: Mitsunobu reaction;
DOI:10.1016/S0040-4020(01)00546-4

Reference yield:

: 316352-94-0
9-(3-iodopropyl)-N⁶-(2-methylpropionyl)adenine

: 316353-30-7
(2S)-benzyloxycarbonylamino-6-[N⁶-(2-methylpropionyl)-9-adeninyl]hexanoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 23 percent / AIBN; Bu₃SnH / toluene / 14 h / 80 °C

2: 89 percent / LiOH*H₂O / tetrahydrofuran; H₂O / 1 h / 0 °C

With lithium hydroxide; 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In tetrahydrofuran; water; toluene;
DOI:10.1016/S0040-4020(01)00546-4