7-[(3aS,4S,6R,6aR)-6-[(tert-butyl(diphenyl)silyl)oxymethyl]-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl]thieno[3,2-d]pyrimidin-4-amine

Base Information

Chemical Name:7-[(3aS,4S,6R,6aR)-6-[(tert-butyl(diphenyl)silyl)oxymethyl]-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl]thieno[3,2-d]pyrimidin-4-amine
CAS No.:1370007-68-3
Molecular Formula:C₃₀H₃₅N₃O₄SSi
Molecular Weight:561.777
Hs Code.:

Synonyms:7-[(3aS,4S,6R,6aR)-6-[(tert-butyl(diphenyl)silyl)oxymethyl]-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl]thieno[3,2-d]pyrimidin-4-amine

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Chemical Property of 7-[(3aS,4S,6R,6aR)-6-[(tert-butyl(diphenyl)silyl)oxymethyl]-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl]thieno[3,2-d]pyrimidin-4-amine

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Technology Process of 7-[(3aS,4S,6R,6aR)-6-[(tert-butyl(diphenyl)silyl)oxymethyl]-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl]thieno[3,2-d]pyrimidin-4-amine

There total 6 articles about 7-[(3aS,4S,6R,6aR)-6-[(tert-butyl(diphenyl)silyl)oxymethyl]-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl]thieno[3,2-d]pyrimidin-4-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: 39.0%

: 1370007-66-1
4-[(3aS,4S,6R,6aR)-6-[(tert-butyl(diphenyl)silyl)oxymethyl]-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl]-3-amino-thiophene-2-carbonitrile

: 3473-63-0
formamidine acetic acid

: 1370007-68-3
7-[(3aS,4S,6R,6aR)-6-[(tert-butyl(diphenyl)silyl)oxymethyl]-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl]thieno[3,2-d]pyrimidin-4-amine

Guidance literature:: With N,N-diethyl-N-isopropylamine; In butan-1-ol; at 150 ℃; for 1.5h; Microwave irradiation;

Reference yield:

: 1370007-65-0
2-((3aS,6R,6aR)-6-(((tert-butyldiphenylsilyl)oxy)methyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-3-(dimethylamino)acrylonitrile

: 1370007-68-3
7-[(3aS,4S,6R,6aR)-6-[(tert-butyl(diphenyl)silyl)oxymethyl]-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl]thieno[3,2-d]pyrimidin-4-amine

Guidance literature:: Multi-step reaction with 4 steps

1: trifluoroacetic acid / chloroform; water / 20 °C

2: triethylamine / dichloromethane / 1.17 h / 0 °C

3: sodium carbonate / ethanol / 6 h / Inert atmosphere; Reflux

4: N,N-diethyl-N-isopropylamine / butan-1-ol / 1.5 h / 150 °C / Microwave irradiation

With N,N-diethyl-N-isopropylamine; sodium carbonate; triethylamine; trifluoroacetic acid; In ethanol; dichloromethane; chloroform; water; butan-1-ol;

Reference yield:

: 1370007-62-7
2-((3aS,6R,6aR)-6-(((tert-butyldiphenylsilyl)oxy)methyl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)acetonitrile

: 1370007-68-3
7-[(3aS,4S,6R,6aR)-6-[(tert-butyl(diphenyl)silyl)oxymethyl]-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl]thieno[3,2-d]pyrimidin-4-amine

Guidance literature:: Multi-step reaction with 5 steps

1: N,N-dimethyl-formamide / 20 °C

2: trifluoroacetic acid / chloroform; water / 20 °C

3: triethylamine / dichloromethane / 1.17 h / 0 °C

4: sodium carbonate / ethanol / 6 h / Inert atmosphere; Reflux

5: N,N-diethyl-N-isopropylamine / butan-1-ol / 1.5 h / 150 °C / Microwave irradiation

With N,N-diethyl-N-isopropylamine; sodium carbonate; triethylamine; trifluoroacetic acid; In ethanol; dichloromethane; chloroform; water; N,N-dimethyl-formamide; butan-1-ol;