{(3aR,4R,6R,6aR)-6-[2-chloro-6-(4-chloro-2-fluoroanilino)-9H-purin-9-yl ]-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl}methanol

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Chemical Name:{(3aR,4R,6R,6aR)-6-[2-chloro-6-(4-chloro-2-fluoroanilino)-9H-purin-9-yl ]-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl}methanol
CAS No.:253127-11-6
Molecular Formula:C₁₉H₁₈Cl₂FN₅O₄
Molecular Weight:470.287
Hs Code.:

Synonyms:{(3aR,4R,6R,6aR)-6-[2-chloro-6-(4-chloro-2-fluoroanilino)-9H-purin-9-yl ]-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl}methanol

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Chemical Property of {(3aR,4R,6R,6aR)-6-[2-chloro-6-(4-chloro-2-fluoroanilino)-9H-purin-9-yl ]-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl}methanol

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Technology Process of {(3aR,4R,6R,6aR)-6-[2-chloro-6-(4-chloro-2-fluoroanilino)-9H-purin-9-yl ]-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl}methanol

There total 5 articles about {(3aR,4R,6R,6aR)-6-[2-chloro-6-(4-chloro-2-fluoroanilino)-9H-purin-9-yl ]-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl}methanol 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: 83.0%

: C₁₆H₁₄Cl₂FN₅O₄

: 77-76-9
2,2-dimethoxy-propane

: 253127-11-6
{(3aR,4R,6R,6aR)-6-[2-chloro-6-(4-chloro-2-fluoroanilino)-9H-purin-9-yl ]-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl}methanol

Guidance literature:: With camphor-10-sulfonic acid; In acetone; at 55 ℃; for 2h;
DOI:10.1021/acs.jmedchem.7b01399

Reference yield:

: 3056-18-6
(2R,3R,4R,5R)-4-(acetyloxy)-2-[(acetyloxy)methyl]-5-(2,6-dichloro-9H-purin-9-yl)tetrahydro-3-furanyl acetate

: 253127-11-6
{(3aR,4R,6R,6aR)-6-[2-chloro-6-(4-chloro-2-fluoroanilino)-9H-purin-9-yl ]-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl}methanol

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / ethanol / 10 h / Reflux

2: ammonia / methanol / 20 °C

3: camphor-10-sulfonic acid / acetone / 2 h / 55 °C

With camphor-10-sulfonic acid; ammonia; triethylamine; In methanol; ethanol; acetone;
DOI:10.1021/acs.jmedchem.7b01399

Reference yield:

: 253127-10-5
(2R,3R,4R,5R)-4-(acetyloxy)-2-[(acetyloxy)methyl]-5-[2-chloro-6-(4-chloro-2-fluoroanilino)-9H-purin-9-yl]tetrahydrofuran-3-yl acetate

: 253127-11-6
{(3aR,4R,6R,6aR)-6-[2-chloro-6-(4-chloro-2-fluoroanilino)-9H-purin-9-yl ]-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl}methanol

Guidance literature:: Multi-step reaction with 2 steps

1: ammonia / methanol / 20 °C

2: camphor-10-sulfonic acid / acetone / 2 h / 55 °C

With camphor-10-sulfonic acid; ammonia; In methanol; acetone;
DOI:10.1021/acs.jmedchem.7b01399