9-((3aR,4R,6R,6aR)-2,2-dimethyl-6-((prop-2-yn-1-ylamino)methyl)tetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-9H-purin-6-amine

Base Information

Chemical Name:9-((3aR,4R,6R,6aR)-2,2-dimethyl-6-((prop-2-yn-1-ylamino)methyl)tetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-9H-purin-6-amine
CAS No.:1383460-52-3
Molecular Formula:C₁₆H₂₀N₆O₃
Molecular Weight:344.373
Hs Code.:

Synonyms:9-((3aR,4R,6R,6aR)-2,2-dimethyl-6-((prop-2-yn-1-ylamino)methyl)tetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-9H-purin-6-amine

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Chemical Property of 9-((3aR,4R,6R,6aR)-2,2-dimethyl-6-((prop-2-yn-1-ylamino)methyl)tetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-9H-purin-6-amine

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Technology Process of 9-((3aR,4R,6R,6aR)-2,2-dimethyl-6-((prop-2-yn-1-ylamino)methyl)tetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-9H-purin-6-amine

There total 1 articles about 9-((3aR,4R,6R,6aR)-2,2-dimethyl-6-((prop-2-yn-1-ylamino)methyl)tetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-9H-purin-6-amine 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: 65.0%

: 21950-36-7
5'-amino-5'-deoxy-2',3'-O-isopropylideneadenosine

: 106-96-7
propargyl bromide

: 1383460-52-3
9-((3aR,4R,6R,6aR)-2,2-dimethyl-6-((prop-2-yn-1-ylamino)methyl)tetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-9H-purin-6-amine

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; toluene; at 0 - 4 ℃; for 18h;

Reference yield:

: 1383460-52-3
9-((3aR,4R,6R,6aR)-2,2-dimethyl-6-((prop-2-yn-1-ylamino)methyl)tetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-9H-purin-6-amine

: 1-(4-(tert-butyl)phenyl)-3-(3-oxopropyl)urea

: C₃₀H₄₀N₈O₄

Guidance literature:: With sodium cyanoborohydride; acetic acid; In ethanol; at 20 - 45 ℃; for 12h; Molecular sieve;
DOI:10.1002/chem.201600259