Technology Process of 10-[(4S,5S,6R)-6-[(3aR,4R,6R,6aR)-6-(tert-Butyl-diphenyl-silanyloxymethyl)-2-(4-methoxy-phenyl)-tetrahydro-furo[3,4-d][1,3]dioxol-4-yloxymethyl]-5-hydroxy-2-(4-methoxy-phenyl)-[1,3]dioxan-4-ylmethyl]-7,8-dimethyl-10H-benzo[g]pteridine-2,4-dione
There total 18 articles about 10-[(4S,5S,6R)-6-[(3aR,4R,6R,6aR)-6-(tert-Butyl-diphenyl-silanyloxymethyl)-2-(4-methoxy-phenyl)-tetrahydro-furo[3,4-d][1,3]dioxol-4-yloxymethyl]-5-hydroxy-2-(4-methoxy-phenyl)-[1,3]dioxan-4-ylmethyl]-7,8-dimethyl-10H-benzo[g]pteridine-2,4-dione 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:
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136738-77-7,136781-02-7
10-[(4S,5S,6R)-6-[(3aR,4S,6R,6aR)-6-(tert-Butyl-diphenyl-silanyloxymethyl)-2-(4-methoxy-phenyl)-tetrahydro-furo[3,4-d][1,3]dioxol-4-yloxymethyl]-5-hydroxy-2-(4-methoxy-phenyl)-[1,3]dioxan-4-ylmethyl]-7,8-dimethyl-10H-benzo[g]pteridine-2,4-dione
- Guidance literature:
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Multi-step reaction with 5 steps
1: 93.2 percent / imidazole / dimethylformamide / 0.5 h / Ambient temperature
2: 90.8 percent / PPTS / CH2Cl2 / 1 h / Ambient temperature
3: 65 percent / sodium benzenesulfinate, KI / dimethylformamide / 6 h / 100 °C
4: 65 percent / DBU / CH2Cl2 / 2 h / 0 °C
5: 35.5 mg / BF3-Et2O / CH2Cl2 / 0 °C
With
1H-imidazole; boron trifluoride diethyl etherate; sodium benzenesulfonate; pyridinium p-toluenesulfonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; potassium iodide;
In
dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4020(01)86553-4
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136738-77-7,136781-02-7
10-[(4S,5S,6R)-6-[(3aR,4R,6R,6aR)-6-(tert-Butyl-diphenyl-silanyloxymethyl)-2-(4-methoxy-phenyl)-tetrahydro-furo[3,4-d][1,3]dioxol-4-yloxymethyl]-5-hydroxy-2-(4-methoxy-phenyl)-[1,3]dioxan-4-ylmethyl]-7,8-dimethyl-10H-benzo[g]pteridine-2,4-dione
- Guidance literature:
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Multi-step reaction with 5 steps
1: 93.2 percent / imidazole / dimethylformamide / 0.5 h / Ambient temperature
2: 90.8 percent / PPTS / CH2Cl2 / 1 h / Ambient temperature
3: 65 percent / sodium benzenesulfinate, KI / dimethylformamide / 6 h / 100 °C
4: 65 percent / DBU / CH2Cl2 / 2 h / 0 °C
5: 10.0 mg / BF3-Et2O / CH2Cl2 / 0 °C
With
1H-imidazole; boron trifluoride diethyl etherate; sodium benzenesulfonate; pyridinium p-toluenesulfonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; potassium iodide;
In
dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4020(01)86553-4
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136738-77-7,136781-02-7
10-[(4S,5S,6R)-6-[(3aR,4S,6R,6aR)-6-(tert-Butyl-diphenyl-silanyloxymethyl)-2-(4-methoxy-phenyl)-tetrahydro-furo[3,4-d][1,3]dioxol-4-yloxymethyl]-5-hydroxy-2-(4-methoxy-phenyl)-[1,3]dioxan-4-ylmethyl]-7,8-dimethyl-10H-benzo[g]pteridine-2,4-dione
- Guidance literature:
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Multi-step reaction with 7 steps
1: 122 g / p-toluenesulfonic acid (pTsOH) / 12 h / Ambient temperature
2: 3.4percent KOH-MeOH / methanol / 3 h / Ambient temperature
3: 93.2 percent / imidazole / dimethylformamide / 0.5 h / Ambient temperature
4: 90.8 percent / PPTS / CH2Cl2 / 1 h / Ambient temperature
5: 65 percent / sodium benzenesulfinate, KI / dimethylformamide / 6 h / 100 °C
6: 65 percent / DBU / CH2Cl2 / 2 h / 0 °C
7: 35.5 mg / BF3-Et2O / CH2Cl2 / 0 °C
With
1H-imidazole; potassium hydroxide; boron trifluoride diethyl etherate; sodium benzenesulfonate; pyridinium p-toluenesulfonate; toluene-4-sulfonic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; potassium iodide;
In
methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4020(01)86553-4